(1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic acid methyl ester

Base Information

Chemical Name:(1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic acid methyl ester
CAS No.:134593-86-5
Molecular Formula:C₂₆H₅₃BrO₅Si₃
Molecular Weight:609.864
Hs Code.:

Synonyms:(1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic acid methyl ester

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Chemical Property of (1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic acid methyl ester

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Technology Process of (1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic acid methyl ester

There total 3 articles about (1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic 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: 100.0%

: 69739-34-0
t-butyldimethylsiyl triflate

: 134593-85-4
(1R,4R,5S,6S)-1-Bromo-4,5,6-trihydroxy-cyclohex-2-enecarboxylic acid methyl ester

: 134593-86-5
(1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic acid methyl ester

Guidance literature:: With 2,6-dimethylpyridine; dmap; In dichloromethane;
DOI:10.1021/jo00014a003

Reference yield:

: 19978-32-6
3-bromo-2H-pyran-2-one

: 134593-86-5
(1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 63 percent / i-Pr₂NEt / CH₂Cl₂ / 4 h / 90 °C

2: 98 percent / p-TsOH / 17 h

3: 100 percent / 4-DMAP, 2,6-lutidine / CH₂Cl₂

With 2,6-dimethylpyridine; dmap; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jo00014a003

Reference yield:

: 134593-84-3,134678-33-4
endo-1-bromo-4,4-dimethyl-3,5,8-trioxatricyclo[5.2.2.0]undec-10-en-9-one

: 134593-86-5
(1S,4S,5R,6R)-1-Bromo-4,5,6-tris-(tert-butyl-dimethyl-silanyloxy)-cyclohex-2-enecarboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / p-TsOH / 17 h

2: 100 percent / 4-DMAP, 2,6-lutidine / CH₂Cl₂

With 2,6-dimethylpyridine; dmap; toluene-4-sulfonic acid; In dichloromethane;
DOI:10.1021/jo00014a003