75415-67-7

Upstream product

• 14204-24-1 N-(phenylthio)succinimide 
• 75415-64-4 8α-benzoyloxymethyl-9β-hydroxy-des-AB-cholestane 
• 75415-62-2 C₄₂H₅₈O₅ 
• 75415-60-0 Acetic acid (3S,5R,8S,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-3-methoxy-5,13-dimethyl-6-oxo-2,3,4,5,6,7,8,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-7-yl ester 
• 75415-59-7 3β-methoxy-5β-methyl-6-trimethylsilyloxy-19-norcholesta-6,9-diene 
• 5226-32-4 6β-acetoxy-3β-methoxy-5β-methyl-19-norcholest-9-ene 
• 5600-02-2 6β-hydroxy-3β-methoxy-5β-methyl-19-norcholest-9-ene 
• 2763-32-8 3β-methoxy-5β-methyl-19-norcholest-9-en-6-one 

Downstream Products

• 3752-57-6 8-hydroxymethyl-des-AB-cholest-8-ene p-nitrobenzoate 
• 75415-66-6 9α-phenylsulphonyl-8α-hydroxymethyl-des-AB-cholestane 
• 75415-68-8 (1R,3aS,4R,5R,7aR)-5-Benzenesulfonyl-1-((R)-1,5-dimethyl-hexyl)-7a-methyl-octahydro-indene-4-carbaldehyde 

Relevant academic research and scientific papers

Calciferol and its Relatives. Part 26. A Conversion of Cholesterol into 8-Hydroxymethyl-des-AB-cholest-8-ene

The methoxy-ketone (7), derived from Westphalen's diol, was degraded to 8α-benzoyloxymethyl-des-AB-cholestan-9-one (10), from which the title compound (6) was obtained in a yield of 47percent based on the ketone (7), or 22.5percent overall from cholestero