(E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic acid methyl ester

Base Information

Chemical Name:(E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic acid methyl ester
CAS No.:372511-40-5
Molecular Formula:C₂₁H₃₄O₅Si
Molecular Weight:394.583
Hs Code.:

Synonyms:(E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic acid methyl ester

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Chemical Property of (E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic acid methyl ester

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Technology Process of (E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic acid methyl ester

There total 5 articles about (E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic 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:

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

: 372511-40-5
(E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: TfOH / diethyl ether

2: LiAlH₄ / tetrahydrofuran

3: iPr₂NEt; LiCl / acetonitrile

With lithium aluminium tetrahydride; trifluorormethanesulfonic acid; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; diethyl ether; acetonitrile; 3: Dess-Martin oxidation / 4: Horner-Wadsworth-Emmons olefination;
DOI:10.1021/ol010150u

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 372511-40-5
(E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: imidazole / CH₂Cl₂

2: TfOH / diethyl ether

3: LiAlH₄ / tetrahydrofuran

4: iPr₂NEt; LiCl / acetonitrile

With 1H-imidazole; lithium aluminium tetrahydride; trifluorormethanesulfonic acid; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; diethyl ether; dichloromethane; acetonitrile; 4: Dess-Martin oxidation / 5: Horner-Wadsworth-Emmons olefination;
DOI:10.1021/ol010150u

Reference yield:

: 372511-48-3
4-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-butan-1-ol

: 372511-40-5
(E)-(R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-hex-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: iPr₂NEt; LiCl / acetonitrile

With N-ethyl-N,N-diisopropylamine; lithium chloride; In acetonitrile; 1: Dess-Martin oxidation / 2: Horner-Wadsworth-Emmons olefination;
DOI:10.1021/ol010150u