(1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester

Base Information

Chemical Name:(1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester
CAS No.:231278-93-6
Molecular Formula:C₂₃H₃₄O₆
Molecular Weight:406.519
Hs Code.:

Synonyms:(1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester

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Chemical Property of (1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester

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Technology Process of (1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester

There total 5 articles about (1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl 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: 99.0%

: 100-39-0
benzyl bromide

: 221344-09-8
(1S,2S,4R,5S)-4,5-Dihydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester

: 231278-93-6
(1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester

Guidance literature:: With tetra-(n-butyl)ammonium iodide; di(n-butyl)tin oxide; In benzene; 1.) reflux, 6 h; 2.) reflux, 3 h;
DOI:10.1002/(SICI)1099-0690(199906)1999:6<1311::AID-EJOC1311>3.0.CO;2-W

Reference yield:

: 51096-08-3
(1S,2S)-cyclohex-4-ene-1,2-dicarboxylic acid

: 231278-93-6
(1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / benzene / Heating

2: 97 percent / OsCl₃, Me₃NO*H₂O / acetone; H₂O / Ambient temperature

3: 99 percent / 1.) Bu₂SnO; 2.) Bu₄NI / benzene / 1.) reflux, 6 h; 2.) reflux, 3 h

With osmium (III) chloride; trimethylamine-N-oxide; tetra-(n-butyl)ammonium iodide; di(n-butyl)tin oxide; In water; acetone; benzene;
DOI:10.1002/(SICI)1099-0690(199906)1999:6<1311::AID-EJOC1311>3.0.CO;2-W

Reference yield:

: 231278-92-5
(1S,2S)-cyclohex-4-ene-1,2-dicarboxylic acid di-tert-butyl ester

: 231278-93-6
(1S,2S,4R,5S)-4-Benzyloxy-5-hydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / OsCl₃, Me₃NO*H₂O / acetone; H₂O / Ambient temperature

2: 99 percent / 1.) Bu₂SnO; 2.) Bu₄NI / benzene / 1.) reflux, 6 h; 2.) reflux, 3 h

With osmium (III) chloride; trimethylamine-N-oxide; tetra-(n-butyl)ammonium iodide; di(n-butyl)tin oxide; In water; acetone; benzene;
DOI:10.1002/(SICI)1099-0690(199906)1999:6<1311::AID-EJOC1311>3.0.CO;2-W