It is a useful solvent due to its polarity, low toxicity, and low vapor pressure. You cannot produce an aliphatic alcohol, but it is possible to produce phenol, which still has the OH group, and then reduce it to a cyclic alcohol. That's the closest you'll get, as far as I can tell. Reaction: Here benzyl chloride is first hydrolyzed to benzyl alcohol, and then undergoes oxidation of a primary alcohol to the corresponding carboxylic acid. I've UTFSE, and I've looked at Rhod's site, and I've searched through the Organic Synthesis site that's linked from Rhod's page, and I couldn't find anything for benzyl alcohol going straight from benzene. It is partially soluble in water and readily soluble in alcohol and ether. Benzyl alcohol is an aromatic alcohol with the formula C 6 H 5 CH 2 OH. To produce a primary alcohol, the Grignard reagent is reacted with formaldehyde. An example is the reduction of methyl benzoate to benzyl alcohol and methanol. Hence in comparison to toluene, benzyl chloride more rapidly oxidizes in presence of an aqueous oxidizing agent. The Grignard reaction is the only simple method available that is capable of producing primary, secondary, and tertiary alcohols. 1. Grignard reaction with aldehydes and ketones. Benzyl alcohol, also called phenylmethanol or phenylcarbinol, is a clear, colorless liquid with a mild pleasant aromatic odor; melting at 15 C and Boiling at 205 C. It is a primary alcohol with arene group. El_Zorro (Hive Addict) 07-17-03 23:38 No 448190 : benzyl alcohol from benzene Bookmark : Does anyone know of a synth of benzyl alcohol from benzene? The benzyl group is often abbreviated "Bn" (not to be confused with "Bz" which is used for benzoyl), thus benzyl alcohol is denoted as BnOH.Benzyl alcohol is a colorless liquid with a mild pleasant aromatic odor. Aim: To prepare benzoic acid from benzyl chloride.


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