CHAPTER 9. Further Reactions of Alcohols and the Chemistry of Ethers

Transcription

1 CHAPTER 9 Further Reactions of Alcohols and the Chemistry of Ethers

2 A variety of reaction modes are available to alcohols.

3 9-1 Reactions of Alcohols with Base: Preparation of Alkoxides Strong bases are needed to deprotonate alcohols completely. Base strength must be stronger than that of the alkoxide.

4 Alkali metals also deprotonate alcohols, but by reduction of H +. Vigorous: Less Vigorous: Relative reactivities:

5 Uses for alkoxides: Hindered alkoxides E 2 reactions with haloalkanes to form alkenes. Less hindered alkoxides S N2 reactions with haloalkanes to form ethers.

6 9-2 Reactions of Alcohols with Strong Acids: Alkyloxonium Ions in Substitution and Elimination Reactions of Alcohols Water has a high pk a (15.7) which means that its conjugate base, OH - is an exceedingly poor leaving group. The OH group of an alcohol must be converted into a better leaving group for alcohols to participate in substitution or elimination reactions.

7 9-2 Reactions of Alcohols with Strong Acids: Alkyloxonium Ions in Substitution and Elimination Reactions of Alcohols Haloalkanes from primary alcohols and HX: Water can be a leaving group. Protonation of the hydroxy substituent of an alcohol to form an alkyloxonium ion converts the OH from the poor leaving group, OH -, to the good leaving group, H 2 O.

8 Primary bromoalkanes and iodoalkanes can be prepared by the reaction with HBr and HI. Chloroalkanes cannot be prepared by this method because Cl - is too poor a nucleophile.

9 Secondary and tertiary alcohols undergo carbocation reactions with acids: S N 1 and E1. Primary alkyloxonium ions undergo only S N 2 reactions with acid. Their carbocation transition state energies are too high to allow S N 1 and E1 reactions under ordinary laboratory conditions. Secondary and tertiary alkyloxonium ions lose water when treated with acid to form a carbocation.

10 When good nucleophiles are present, the S N 1 mechanism predominates. Here the tertiary carbocation is generated at a relatively low temperature, which prevents the competing E 1 reaction. At higher temperatures, or in the absence of good nucleophiles, elimination becomes dominant.

11 Secondary alcohols show complex behavior when treated with HX, following S N 2, S N 1, and E1 pathways. Relatively hindered (compared to primary alcohols): Retarded S N 2 reactivity Slow to form carbocations (compared to tertiary alcohols): Retarded S N 1 reactivity.

12 E1 reactions of alcohols (dehydrations) result in the formation of alkenes. Non-nucleophilic acids, such as H 3 PO 4 or H 2 SO 4, are used in this case, rather than the nucleophilic acids, HBr and HI. Dehydrations of tertiary alcohols often occur just above room temperature.

13 Summary

14 9-3 Carbocation Rearrangements Hydride shifts give new S N 1 products. Treatment of substituted secondary alcohols produces unexpected results:

15 Rearrangement of an initial secondary carbocation to the more stable tertiary carbocation by a hydride shift results in a rearranged product.

16 Hydride shifts are very fast (faster than S N 1 or E1) which is partially due to hyperconjugation in the carbocation weakening the C-H bond):

17 Primary carbocations are too unstable to be formed by rearrangement. Secondary or tertiary carbocations equilibrate readily, leading to a mixture of products when trapped by a nucleophile.

18 Carbocation rearrangement takes place regardless of the precursor leading to the carbocation.

19 Carbocation rearrangements also give new E1 products. Under conditions favoring elimination (elevated temperatures and nonnucleophilic media), carbocations can also rearrange to give rearranged products.

20 Other carbocation rearrangements are due to alkyl shifts. Alkyl shifts, rather than hydride shifts, can occur when a carbocation lacks a suitable secondary or tertiary hydrogen next to the positively charged carbon.

21 Alkyl and hydride shifts are faster when leading to a tertiary carbocation than when leading to a secondary carbocation. In the previous haloalkane rearrangement, movement of an ethyl group rather than a hydride would result in a secondary rather than a tertiary carbocation. Exceptions to this general rule can occur as a result of electronic stabilization or steric relief.

22 Primary alcohols may undergo rearrangement. Alkyl and hydride shifts to primary carbons bearing leaving groups can occur without the formation of primary carbocations. In this case, steric hindrance interferes with direct attack by the bromide ion. Instead, water leaves at the same time as the methyl group migrates, bypassing the formation of a primary carbocation.

23 9-4 Organic and Inorganic Esters from Alcohols Organic esters are derivatives of carboxylic acids. Inorganic esters are the analogous derivatives of inorganic acids.

24 9-4 Organic and Inorganic Esters from Alcohols Alcohols react with carboxylic acids to give organic esters. Esterification is the reaction of alcohols with carboxylic acids in the presence of catalytic amounts of a strong inorganic acid (H 2 SO 4 or HCl) which yields esters and water. This is an equilibrium process which can be shifted in either direction.

25 Haloalkanes can be made from alcohols through inorganic esters. As an alternative to the acid-catalyzed conversions of alcohols into haloalkanes, a number of inorganic reagents can convert the alcoholic hydroxyl group into a good leaving group under milder conditions. The reaction of PBr 3 with a secondary alcohol yields a bromoalkane and phosphorous acid (all three bromine atoms can be utilized).

26

27 Iodoalkanes can be prepared using PI 3, which, because of its reactivity, is generated from red phosphorous and iodine in the reaction mixture itself.

28 Chloroalkanes are commonly prepared using thionyl chloride by warming an alcohol in its presence. An amine such as triethyl amine is usually added to consume the generated HCl.

29 Alkyl sulfonates are versatile substrates for substitution reactions. Alkyl sulfonates are excellent leaving groups and can be generated by the reaction of an alcohol with the corresponding sulfonyl chloride. Pyridine or a tertiary amine is used to remove the HCl formed. Alkyl sulfonates are often crystalline solids and can be isolated and purified before further reaction.

30 The sulfonate group can be displaced by halide ions (particularly in primary and secondary systems). The sulfonate group can also be displaced by any good nucleophile, not just by halide ions as was the case for hydrogen, phosphorous, and thionyl halides.

31 9-5 Names and Physical Properties of Ethers In the IUPAC system, ethers are alkoxyalkanes. IUPAC: Ethers are alkanes bearing an alkoxy substituent. The larger substituent is the stem and the smaller substituent is the alkoxy group (methoxyethane). Common Names: The names of the two alkyl groups are followed by the word ether (ethylmethylether).

32 Except for strained cyclical derivatives, ethers are fairly unreactive and are often used as solvents in organic reactions. Cyclic ethers are members of the class of cycloalkanes called heterocycles, in which one or more carbon atoms have been replaced by a heteroatom.

33 Cyclic ethers names are based on the oxacycloalkane stem: Oxacyclopropane (oxiranes, epoxides, ethylene oxides) Oxacyclobutane Oxacyclopentane (tetrahydrofurans) Oxacyclohexanes (tetrahydropyrans) Ring numbering starts on the oxygen atom.

34 Cyclic polyethers based on the 1,2-ethanediol unit are called crown ethers. The crown ether 18-crown-6 contains 18 total atoms and 6 oxygen atoms. Note that the inside of the ring is electron rich.

35 The absence of hydrogen bonding affects the physical properties of ethers. Simple alkoxyalkanes have the same molecular formula as the equivalent alkanols, C n H 2n+2 O, but have much lower boiling points due to the absence of hydrogen bonding.

36 The smaller alkoxyalkanes are water soluble, however solubility decreases with increasing hydrocarbon size. Methoxymethane completely water soluble Ethoxyethane 10% aqueous solution

37 Polyethers solvate metal ions: crown ethers and ionophores. Crown ethers can render salts soluble in organic solvents by chelating the metal cations. This allows reagents such as KMnO 4 to act as an oxidizing agent in the organic solvents. The size of the central cavity can be tailored to selectively bind cations of differing ionic radii.

38 Three-dimensional analogs of crown ethers are polyethers called cryptands. These are highly selective in alkali and other metal cation binding.

39 9-6 Williamson Ether Synthesis Ethers are prepared by S N 2 reactions. Ethers can be prepared by the reaction of an alkoxide with a primary haloalkane or sulfonate ester under S N 2 conditions. The parent alcohol of the alkoxide can be used as the solvent, however other polar solvents are often better, such as DMSO (dimethyl sulfoxide) or HMPA (hexamethylphosphoric triamide).

40 The use of alkoxides in ether synthesis is restricted to primary unhindered alkylating agents, otherwise significant amounts of E2 products are formed.

41 Cyclic ethers can be prepared by intramolecular Williamson synthesis. Haloalcohols serve as the starting point for the Williamson synthesis of cyclic ethers. The intramolecular reaction is usually much faster than the intermolecular reaction. If necessary, the intermolecular reaction can be suppressed by using a high dilution of the haloalcohol.

42 Cyclic ethers of even small rings can be prepared using the Williamson synthesis.

43 Ring size controls the speed of cyclic ether formation. The rate of ring closure is based on both enthalpic and entropic contributions. These rate differences can be explained based on the interplay between strain, entropy, and proximity. Entropy reduction (due to ring closure) increases with increasing ring size. (Reaction rate decrease with increasing ring size.) Ring strain decreases with increasing ring size. (Reaction rate increase with increasing ring size.) Transition-state strain is reduced in the 2-haloalkoxides because the 2-haloalkoxide is already strained by the proximity of the halide and hydroxyl. (Reaction rate increase for the 2-haloalkoxides.)

44 The intramolecular Williamson synthesis is stereospecific. Since the Williamson synthesis is a S N 2 substitution reaction, an inversion of configuration occurs at the carbon bearing the leaving group. The leaving group must be on the opposite side of the molecule from the attacking nucleophile in order for the reaction to occur.

45 9-7 Synthesis of Ethers: Alcohols and Mineral Acid Alcohols give ethers by both S N 2 and S N 1 mechanisms. Strong nucleophilic acids (HBr, HI) yield haloalkanes when reacted with alcohols. Strong non-nucleophilic acids yields ethers when reacted with alcohols.

46 At higher temperatures, an E2 elimination of water occurs with the subsequent production of alkenes. Secondary and tertiary alcohols form ethers through an S N 1 reaction with a second molecule of the alcohol trapping the carbocation. The E1 pathway becomes dominate at higher temperatures.

47 Mixed ethers containing one tertiary and one primary or secondary alcohol can be prepared in the presence of dilute acid. The tertiary carbocation is trapped by the less hindered alcohol.

48 Ethers also form by alcoholysis. This occurs by simply dissolving a tertiary or secondary haloalkane in an alcohol and waiting until the S N 1 process is complete.

49 9-8 Reactions of Ethers Ethers are usually inert, however, they do react slowly with oxygen to form hydroperoxides and peroxides which can decompose explosively.

50 9-8 Reactions of Ethers The ether oxygen atom can be protonated to generate alkyloxonium ions. With primary groups and strong nucleophilic acids (HBr), S N 2 displacement takes place.

51 Oxonium ions from secondary ethers may transform by either S N 2 or S N 1 reactions, depending upon conditions.

52 Tertiary ethers are protecting groups for alcohols. Esters containing tertiary alkyl groups react in dilute acid to give carbocations which are either trapped (S N 1) by good nucleophiles or deprotonated in the absence of good nucleophiles. Because they are readily formed (and equally readily hydrolyzed), tertiary ethers are commonly used as protecting groups during chemical reactions which might otherwise interact with the unprotected alcohol.

53 9-9 Reactions of Oxacyclopropanes Nucleophilic ring opening of oxacyclopropanes by S N 2 is regioselective and stereospecific. Oxacyclopropane can be ring-opened by anionic nucleophiles. Because the molecule is symmetric, nucleophilic attack can be at either carbon atom. The driving force for this reaction is the release of ring strain.

54 With unsymmetric systems, attack will be at the less substituted carbon center. This selectivity is referred to as regioselectivity. If the ring opens at a stereocenter, inversion is observed.

55 Hydride and organometallic reagents convert strained ethers into alcohols. LiAlH 4 can open the rings of oxacyclopropanes to yield alcohols. (Ordinary ethers do not react.) In asymmetrical systems, the hydride attacks the less substituted side.

56 If the reacting carbon is a stereocenter, inversion is observed.

57 Oxacyclopropanes are sufficiently reactive electrophiles to be attacked by organometallic compounds.

58 Acids catalyze oxacyclopropane ring opening. Ring opening of oxacyclopropane by acid catalysis proceeds through an initial cyclic alkyloxonium ion. This acid catalyzed ring opening is both regioselective and stereospecific.

59 The acid catalyzed methanolysis of 2,2-dimethyloxacyclopropane is ring-opened at the more hindered carbon.

60 In the alkyloxonium ion, more positive charge is located on the tertiary carbon than on the primary carbon. This effect counteracts the effect of steric hindrance and the alcohol attacks the tertiary carbon. Because inversion of configuration occurs during ring opening, free carbocations cannot be involved in the reaction mechanism.

61 9-10 Sulfur Analogs of Alcohols and Ethers The sulfur analogs of alcohols and ethers are thiols and sulfides. The IUPAC system calls the sulfur analogs of alcohols, R-SH, thiols. The SH group in more complicated compounds is referred to as mercapto.

62 The sulfur analogs of ethers are called sulfides (common name, thioethers). The RS group is called alkylthio, and the RS - group is called alkanethiolate.

63 Thiols are less hydrogen-bonded and more acidic than alcohols. Compared to oxygen, sulfur has a large size, diffuse orbitals and a relatively nonpolarized S-H bond. The boiling points of thiols are similar to those of the analogous haloalkanes.

64 Thiols are more acidic than water and can therefore be easily deprotonated by hydroxide and alkoxide ions:

65 Thiols and sulfides react much like alcohols and ethers. The sulfur in thiols and sulfides is more nucleophilic than the oxygen in the analogous compounds. Thiols and sulfides are readily made through nucleophilic attack by RS - or HS - on haloalkanes: A large excess of HS - is used to prevent the reaction of the product with the starting halide.

66 Sulfides are prepared by the alkylation of thiols in the presence of a base, such as hydroxide. The nucleophilicity of the generated thiolates is much greater than that of hydroxide which eliminates the competing S N 2 substitution by hydroxide ion.

67 Sulfides can attack haloalkanes to form sulfonium ions. Sulfonium ions are subject to nucleophilic attack, the leaving group being a sulfide.

68 Valence-shell expansion of sulfur accounts for the special reactivity of thiols and sulfides. Sulfur can expand its valence shell from 8 to 10 or 12 electrons using its available 3d orbitals, allowing oxidation states not available to its oxygen analogs. Oxidation of thiols with strong oxidizing agents (H 2 O 2, KMnO 4 ) gives the corresponding sulfonic acids:

69 Milder oxidizing agents (I 2 ) yield disulfides. These can be reduced back to thiols by alkali metals. Reversible disulfide formation is important in stabilizing the folding of biological enzymes:

70 Sulfides can also be oxidized to sulfoxides and then sulfones:

71 9-11 Physiological Properties and Uses of Alcohols and Ethers Methanol: Formed by catalytic reduction of CO and H 2 at high temperatures and pressure. Used as a solvent, a fuel for camp stoves and soldering torches, and as a synthetic intermediate. Highly poisonous. May lead to blindness or death. A possible precursor of gasoline.

72 Ethanol: Alcohol in alcoholic beverages General depressant High in calories, little nutritional value Metabolically degraded linearly with time Poisonous (lethal concentration ~ 0.4%) Near toxic dose used to treat methanol poisoning Produced by fermentation of sugars and starch Commercially produced by the hydration of ethylene. Used as a solvent, a synthetic intermediate, and as a gasoline additive (gasahol)

73 2-Propanol: Toxic, but not absorbed through the skin Used as a rubbing alcohol, a solvent, and as a cleaning agent 1,2-Ethanediol (ethylene glycol): Used as an antifreeze (completely miscible with water) Produced from ethene:

74 1,2,3-Propanetriol (glycerol, glycerine): Non-toxic Major component of fatty tissue Liberated by the action of alkali on fats to form soaps: Phosphoric esters of glycerols are major cell membrane components. Used in lotions, cosmetics, and medicinal preparations.

75 Forms nitroglycerine upon treatment with nitric acid. Cholesterol: An important steroid alcohol Ethoxyethane (diethyl ether): Formally used as an anesthetic Explosive when mixed with air

76 Oxacyclopropane (oxirane, ethylene oxide) Industrial chemical intermediate Fumigating agent for seeds and grains Oxacyclopropane derivatives control insect metamorphosis and are formed during enzyme-catalyzed oxidations of aromatic hydrocarbons (highly carcinogenic). Alcohol and ether groups are found in natural products such as morphine and tetrahydrocannabinol:

77 Lower MW thiols and sulfides are notorious for their foul smells. The odor of the skunk s defensive spray are thiols and a sulfide: When highly diluted, thiols and sulfides have a pleasant odor: freshly chopped onion or garlic, black tea, grapefruit. The compound responsible for the taste of grapefruit can be tasted in concentrations in the ppb range:

78 Drugs such as the sulfonamides (sulfa drugs) contain sulfur in their molecular framework:

79 9 Important Concepts 1. Reactivity of ROH With Alkali Metals R = CH 3 > primary > secondary > tertiary 2. Reactions with Acid and a Nucleophilic Counterion Primary Alcohols S N 2 reactions Secondary and Tertiary Alcohols Form carbocations capable of E1 and S N 1 reactions, before and after rearrangement 3. Carbocation Rearrangements Hydride and alkyl group shifts Result in interconversion of secondary carbocations or conversion of secondary to tertiary carbocation Primary alkyloxonium can rearrange to secondary or tertiary carbocations

80 9 Important Concepts 4. Haloalkane Synthesis Methods using inorganic esters yield primary and secondary haloalkanes with less chance of rearrangement. 5. Ether Preparation Williamson ether synthesis Best when S N 2 reactivity is high Reaction of alcohols with strong non-nucleophilic acids elimination completes at higher temperatures 6. Crown Ethers and Cryptands Examples of ionophores which solubilize metal ions in hydrophobic media.

81 9 Important Concepts 7. Ring Opening of Oxacyclopropanes Nucleophilic attack at the less substituted ring carbon Acid-catalyzed attack favors the more substituted ring carbon 8. Sulfur More diffuse orbitals than oxygen The thiol S-H bond is less polarized than the O-H bond in alcohols (less hydrogen bonding) Acidity of S-H is greater than O-H