(E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol

Base Information

Chemical Name:(E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol
CAS No.:303158-66-9
Molecular Formula:C₂₅H₃₆O₅Si
Molecular Weight:444.643
Hs Code.:

Synonyms:(E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol

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Chemical Property of (E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol

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Technology Process of (E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol

There total 6 articles about (E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-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: 89.0%

: 303158-52-3
tert-Butyl-[(E)-(R)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxymethoxy-3-methyl-but-2-enyloxy]-diphenyl-silane

: 303158-66-9
(E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol

Guidance literature:: With acetic acid;
DOI:10.1021/ol0063656

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 303158-66-9
(E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol

Guidance literature:: Multi-step reaction with 6 steps

1.1: 98 percent / imidazole / dimethylformamide

2.1: CH₂Cl₂

2.2: 98 percent / Me₂S

3.1: 96 percent / toluene / Heating

4.1: 95 percent / DIBAL / CH₂Cl₂ / 0 °C

5.1: 94 percent / i-Pr₂NEt / CH₂Cl₂

6.1: 89 percent / aq. AcOH

With 1H-imidazole; diisobutylaluminium hydride; acetic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; toluene; 1.1: silylation / 2.1: ozonation / 2.2: Reduction / 3.1: Wittig olefination / 4.1: Reduction / 5.1: Alkylation / 6.1: Hydrolysis;
DOI:10.1021/ol0063656

Reference yield:

: 209479-86-7
(2R,3R)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol

: 303158-66-9
(E)-(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxy)-6-methoxymethoxy-5-methyl-hex-4-ene-1,2-diol

Guidance literature:: Multi-step reaction with 5 steps

1.1: CH₂Cl₂

1.2: 98 percent / Me₂S

2.1: 96 percent / toluene / Heating

3.1: 95 percent / DIBAL / CH₂Cl₂ / 0 °C

4.1: 94 percent / i-Pr₂NEt / CH₂Cl₂

5.1: 89 percent / aq. AcOH

With diisobutylaluminium hydride; acetic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane; toluene; 1.1: ozonation / 1.2: Reduction / 2.1: Wittig olefination / 3.1: Reduction / 4.1: Alkylation / 5.1: Hydrolysis;
DOI:10.1021/ol0063656