3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl ester

Base Information

Chemical Name:3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl ester
CAS No.:287411-66-9
Molecular Formula:C₃₆H₄₄O₅SeSi₂
Molecular Weight:691.873
Hs Code.:

Synonyms:3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl ester

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Chemical Property of 3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl ester

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Technology Process of 3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl ester

There total 4 articles about 3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl 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:

: 3-hydroxy-2-(phenylselanyl)butyric acid tert-butyl ester

: 287411-57-8
1-chloro-2,2-dimethyl-1,1-di(4-methoxy-phenyl)-2-phenyl-disilane

: 287411-66-9
3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl ester

Guidance literature:: With 1H-imidazole; dmap; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1021/jo000041d

Reference yield:

: 18414-51-2
di(4-methoxy-phenyl)dichlorosilane

: 287411-66-9
3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / tetrahydrofuran / 4 h / 0 °C

2.1: lithium / tetrahydrofuran / 0 °C

2.2: tetrahydrofuran / 1 h / 0 °C

3.1: acetyl chloride / CH₂Cl₂ / 2 h

4.1: imidazole; DMAP / dimethylformamide / 12 h / 20 °C

With 1H-imidazole; dmap; lithium; triethylamine; acetyl chloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1.1: Substitution / 2.1: Metallation / 2.2: Substitution / 3.1: Substitution / 4.1: silylation;
DOI:10.1021/jo000041d

Reference yield:

: (chlorodi(4-methoxy-phenyl)silanyl)diethyl amide

: 287411-66-9
3-[di(4-methoxyphenyl)-trimethylsilyl-silyloxy]-2-phenylselanyl-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium / tetrahydrofuran / 0 °C

1.2: tetrahydrofuran / 1 h / 0 °C

2.1: acetyl chloride / CH₂Cl₂ / 2 h

3.1: imidazole; DMAP / dimethylformamide / 12 h / 20 °C

With 1H-imidazole; dmap; lithium; acetyl chloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1.1: Metallation / 1.2: Substitution / 2.1: Substitution / 3.1: silylation;
DOI:10.1021/jo000041d