(2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol

Base Information

Chemical Name:(2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol
CAS No.:334972-55-3
Molecular Formula:C₂₀H₃₆O₅Si
Molecular Weight:384.588
Hs Code.:

Synonyms:(2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol

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Technology Process of (2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol

There total 5 articles about (2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol 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: 93.0%

: 334972-54-2
(S)-tert-butyl((2-((4-methoxybenzyl)oxy)hex-5-en-1-yl)oxy)dimethylsilane

: 334972-55-3
(2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol

Guidance literature:: With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In water; acetone; tert-butyl alcohol; at 20 ℃; for 40h;
DOI:10.1039/b100777g

Reference yield:

: 127102-61-8
(S)-hex-5-ene-1,2-diol

: 334972-55-3
(2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / Et₃N; DMAP / CH₂Cl₂ / 20 °C

2: 90 percent / CF₃SO₃H / diethyl ether / 0.5 h / 20 °C

3: 93 percent / N-methylmorpholine N-oxide; OsO₄ / 2-methyl-propan-2-ol; acetone; H₂O / 40 h / 20 °C

With dmap; osmium(VIII) oxide; trifluorormethanesulfonic acid; 4-methylmorpholine N-oxide; triethylamine; In diethyl ether; dichloromethane; water; acetone; tert-butyl alcohol;
DOI:10.1039/b100777g

Reference yield:

: 89238-99-3
O-(4-methoxybenzyl)-trichloroacetimidate

: 334972-55-3
(2RS,5S)-6-(tert-Butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)hexane-1,2-diol

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / CF₃SO₃H / diethyl ether / 0.5 h / 20 °C

2: 93 percent / N-methylmorpholine N-oxide; OsO₄ / 2-methyl-propan-2-ol; acetone; H₂O / 40 h / 20 °C

With osmium(VIII) oxide; trifluorormethanesulfonic acid; 4-methylmorpholine N-oxide; In diethyl ether; water; acetone; tert-butyl alcohol;
DOI:10.1039/b100777g