(Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene

Base Information

Chemical Name:(Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene
CAS No.:1057668-40-2
Molecular Formula:C₂₀H₂₉Cl₃O₃Si
Molecular Weight:451.893
Hs Code.:

Synonyms:(Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene

Suppliers and Price of (Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene

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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 (Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene

Chemical Property:

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Technology Process of (Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene

There total 1 articles about (Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene 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: 90.0%

: 1057668-31-1
(Z)-6-(tert-butyldimethylsilyloxy)-1-phenylhex-4-en-3-ol

: 4124-31-6
trichloroacetic acid anhydride

: 1057668-40-2
(Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene

Guidance literature:: With pyridine; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ja804167v

Reference yield: 12.0%

: 1057668-40-2
(Z)-6-(tert-butyldimethylsilyloxy)-3-trichloroacetoxy-1-phenylhex-4-ene

: (3RS,4RS,5RS)-6-(tert-butyldimethylsilyloxy)-4,5-dichloro-3-trichloroacetoxy-1-phenylhexane

: (3RS,4SR,5SR)-6-(tert-butyldimethylsilyloxy)-4,5-dichloro-3-trichloroacetoxy-1-phenylhexane

Guidance literature:: With tetraethylammonium trichloride; In dichloromethane; at -90 - 0 ℃; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/ja804167v