(1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester

Base Information

Chemical Name:(1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester
CAS No.:326599-70-6
Molecular Formula:C₂₆H₃₆O₆SSi
Molecular Weight:504.72
Hs Code.:

Synonyms:(1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester

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Chemical Property of (1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester

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Technology Process of (1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester

There total 8 articles about (1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 326599-69-3
methyl (1S,3S,4R,5S)-3-(tert-butyldiphenylsilyloxy)-5-hydroxy-4-methylcyclohexane-1-carboxylate

: 124-63-0
methanesulfonyl chloride

: 326599-70-6
(1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 3h;
DOI:10.1002/ejoc.200500289

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 326599-70-6
(1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 89 percent / imidazole; DMAP / dimethylformamide / 10 h / 20 °C

2: 98 percent / K₂CO₃ / methanol / 6 h / 20 °C

3: 90 percent / DMAP; Et₃N / CH₂Cl₂ / 10 h / 0 °C

4: 55 percent / 18-crown-6 / 2.5 h / 110 °C

5: 98 percent / K₂CO₃ / methanol / 6 h / 20 °C

6: 92 percent / Et₃N / CH₂Cl₂ / 3 h / 0 °C

With 1H-imidazole; dmap; 18-crown-6 ether; potassium carbonate; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.200500289

Reference yield:

: 326598-95-2
(1R,3S,4S,5R)-5-acetoxy-3-hydroxy-4-methyl-1-(methoxycarbonyl)cyclohexane

: 326599-70-6
(1R,3S,4S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-methanesulfonyloxy-4-methyl-cyclohexanecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 89 percent / imidazole; DMAP / dimethylformamide / 10 h / 20 °C

2: 98 percent / K₂CO₃ / methanol / 6 h / 20 °C

3: 90 percent / DMAP; Et₃N / CH₂Cl₂ / 10 h / 0 °C

4: 55 percent / 18-crown-6 / 2.5 h / 110 °C

5: 98 percent / K₂CO₃ / methanol / 6 h / 20 °C

6: 92 percent / Et₃N / CH₂Cl₂ / 3 h / 0 °C

With 1H-imidazole; dmap; 18-crown-6 ether; potassium carbonate; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.200500289