Benzoin hydrogenation

C6H5CH(0H)CN I HCOCgHi - C6H5CH(OH)COC H, - HCN unchanged benzaldehyde, giving benzoin and regenerating the hydrogen cyanide... 

The cyclic carbonate of benzoin (4,5-diphenyl-l,3-dioxol-2-one, prepared from benzoin and phosgene) blocks both hydrogen atoms of primary amines after dehydration acid stable, easily crystallizable Sheehan oxazolinones are formed, which are also called Ox derivatives. The amine is quantitatively deblocked by catalytic hydrogenation in the presence of 1 equiv. of aqueous acid (J.C Sheehan, 1972, 1973 M.J. Miller, 1983). An intelligent application to syntheses of acid labile -lactams is given in the previous section (p. 161). 

Benzoin -As a small cjnantity of potassium cyanide is (apable of converting a large quantity of benzaldehyde into bciv/oin, the action of the cyanide has been explained as follows. The potassium cyanide first reacts with the aldehyde and forms a cyanhydnn, which then condenses with another molecule of aldehyde, hydrogen cyanide being finally eliminated (Lapwortbj,... 

Benzoin and a wide variety of related compounds (e.g. 12, 70-74) have been extensively studied both as initiators of polymerization and in terms of their general photochemistry.271 2 3 The acetophenone chromophore absorbs in the near UV (300-400 nm). In the absence of hydrogen atom donors the mechanism of... 

It should be pointed out that not all benzoin derivatives (75) are suitable for use as photoinitialors. Benzoin esters (75, R=aeyl) undergo a side reaction leading to furan derivatives. Aryl ethers (75, R=aryl) undergo (3-seission to give a phenoxy radical (an inhibitor) in competition with a-scission (Scheme 3.54). Benzoin derivatives with a-hydrogens (75 R-Il) are readily autoxidized and consequently can have poor shelf lives. 

Only a few other cobalt complexes of the type covered in this review (and therefore excluding, for example, the cobalt carbonyls) have been reported to act as catalysts for homogeneous hydrogenation. The complex Co(DMG)2 will catalyze the hydrogenation of benzil (PhCOCOPh) to benzoin (PhCHOHCOPh). When this reaction is carried out in the presence of quinine, the product shows optical activity. The degree of optical purity varies with the nature of the solvent and reaches a maximum of 61.5% in benzene. It was concluded that asymmetric synthesis occurred via the formation of an organocobalt complex in which quinine was coordinated in the trans position (133). Both Co(DMG)2 and cobalamin-cobalt(II) in methanol will catalyze the following reductive methylations ... 

A mechanistic rationale for the observed cw-selectivity has been proposed based on preorganisation of the Breslow-type intermediate and imine through hydrogen bonding 253, with an aza-benzoin oxy-Cope process proposed. Reaction via a boat transition state delivers the observed cw-stereochemistry of the product (Scheme 12.57). Related work by Nair and co-workers (using enones 42 in place of a,P-unsaturated sulfonylimines 251, see Section 12.2.2) generates P-lactones 43 with fran -ring substituents, while the P-lactam products 252 possess a cw-stereo-chemical relationship. 

The reaction in THF requires comments. In THF, the reaction may not be true grafting. THF is known to be very susceptible to hydrogen abstraction and furthermore, benzoin isoproply ether... 

Hydrogen sulfide is introduced into an ice-cooled solution of 0.2 mol of a 1,2-diketone and 0.02 mol of piperidine in 30 ml of dimethylformamide for 1 -4 hours. Elemental sulfur is precipitated during the introduction of hydrogen sulfide. The mixture is acidified with dilute hydrochloric acid the sediment is filtered with suction and dissolved in warm methanol the undissolved sulfur is separated, and the product is isolated by evaporation of the methanol and purified by crystallization. If the product after the acidification is liquid it is isolated by ether extraction and distillation after drying of the ether extract with sodium sulfate. Yield of benzoin from benzil after 1 hour of treatment with hydrogen sulfide is quantitative. 

If hydrogen sulfide is introduced for 4 hours into a solution of 0.2 mol of an a-diketone in methanol and 0.02 mol of pyridine, a monoketone is obtained. The yield of deoxybenzoin from benzoin is quantitative. 

Hydrogen peroxide Peroxodisulfates Diacyl peroxides Hydroperoxides Peracid ester Ag+,Fe2+,Co +,Tp+ Hydrogen sulfites, sulfites, thiosulfates, mercaptans, sulfinic acids Amines (e.g. NdV-dimethylaniline), certain sugars Benzoin/Fe Hydrogen sulfite/Fe ... 

Benzene was discovered in 1825 by Michael Faraday who identified it from a liquid residue of heated whale oil. Faraday called the compound bicarburet of hydrogen and its name was later changed to benzin by Eilhardt Mitscherlich (1794—1863) who isolated the compound from benzoin. Benzene s formula indicates it is highly unsaturated. This would suggest benzene... 

Nucleophilic addition to C=0 (contd.) ammonia derivs., 219 base catalysis, 204, 207, 212, 216, 226 benzoin condensation, 231 bisulphite anion, 207, 213 Cannizzaro reaction, 216 carbanions, 221-234 Claisen ester condensation, 229 Claisen-Schmidt reaction, 226 conjugate, 200, 213 cyanide ion, 212 Dieckmann reaction, 230 electronic effects in, 205, 208, 226 electrons, 217 Grignard reagents, 221, 235 halide ion, 214 hydration, 207 hydride ion, 214 hydrogen bonding in, 204, 209 in carboxylic derivs., 236-244 intermediates in, 50, 219 intramolecular, 217, 232 irreversible, 215, 222 Knoevenagel reaction, 228 Lewis acids in, 204, 222 Meerwein-Ponndorf reaction, 215 MejSiCN, 213 nitroalkanes, 226 Perkin reaction, 227 pH and, 204, 208, 219 protection, 211... 

Desoxybenzoin has been prepared by treatment of bromo-stilbene with water in a sealed tube at 180-190° 1 by the reduction of benzoin 2 by the reduction of benzil 3 by the action of zinc and alcoholic hydrogen chloride on chlorobenzil 4 by the action of benzene on phenylacetic acid in the presence of phosphorus pentoxide 5 and by the action of benzene on phenylacetyl chloride in the presence of aluminum chloride.6... 

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