(4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one

Base Information

Chemical Name:(4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one
CAS No.:202859-87-8
Molecular Formula:C₂₄H₄₂O₅Si₂
Molecular Weight:466.765
Hs Code.:

Synonyms:(4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one

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Chemical Property of (4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one

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Technology Process of (4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one

There total 6 articles about (4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one 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: 98.0%

: 94124-39-7
tert-butylphenylmethoxysilyl bromide

: 191410-05-6
(4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-hydroxy-7-methyl-oxepan-2-one

: 202859-87-8
(4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one

Guidance literature:: With triethylamine; N,N-dimethyl-formamide; In dichloromethane; for 6h; Ambient temperature;

Reference yield:

: 191410-00-1
(2R,3R,5R)-3-tert-butyldimethylsilyloxy-2-methyl-5-(1-methylethenyl)cyclohexanone

: 202859-87-8
(4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: KIO₄, OsO₄ / tetrahydrofuran; H₂O / 12 h

2: 70 percent / MCPBA / CH₂Cl₂ / 144 h / Ambient temperature

3: 78 percent / acetone; H₂O; various solvent(s) / 35 °C / PLE (EC 3.1.1.1)

4: 98 percent / Et₃N, DMF / CH₂Cl₂ / 6 h / Ambient temperature

With osmium(VIII) oxide; potassium metaperiodate; triethylamine; N,N-dimethyl-formamide; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; water; acetone;

Reference yield:

: 191410-02-3
Acetic acid (1R,3R,4R)-3-(tert-butyl-dimethyl-silanyloxy)-4-methyl-5-oxo-cyclohexyl ester

: 202859-87-8
(4R,6R,7R)-6-(tert-Butyl-dimethyl-silanyloxy)-4-(tert-butyl-methoxy-phenyl-silanyloxy)-7-methyl-oxepan-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / MCPBA / CH₂Cl₂ / 48 h / Ambient temperature

2: 78 percent / acetone; H₂O; various solvent(s) / 35 °C / PLE (EC 3.1.1.1)

3: 98 percent / Et₃N, DMF / CH₂Cl₂ / 6 h / Ambient temperature

With triethylamine; N,N-dimethyl-formamide; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; water; acetone;