(4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-2-one

Base Information

Chemical Name:(4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-2-one
CAS No.:445483-89-6
Molecular Formula:C₃₁H₃₅NO₄Si
Molecular Weight:513.709
Hs Code.:

Synonyms:(4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-2-one

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Chemical Property of (4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-2-one

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Technology Process of (4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-2-one

There total 3 articles about (4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-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: 70.0%

: 92817-88-4
(2S)-3-{[tert-butyl(diphenyl)silyl]oxy}-2-methylpropanal

: 201340-02-5
(4S)-3-[(diethylphosphoro)-acetyl]-4-phenyl-2-oxazolidinone

: 445483-89-6
(4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-2-one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; lithium chloride; In acetonitrile; at 20 ℃; for 24h;
DOI:10.1002/ejoc.200600154

Reference yield:

: 95514-03-7
(S)-3-(tert-butyl-diphenyl-silanyloxy)-2-methyl-propionic acid methyl ester

: 445483-89-6
(4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / DIBAL-H / toluene; diethyl ether / 1.25 h / -80 °C

2: 70 percent / (i-Pr)2NEt; LiCl / acetonitrile / 24 h / 20 °C

With diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; lithium chloride; In diethyl ether; toluene; acetonitrile;
DOI:10.1002/ejoc.200600154

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 445483-89-6
(4S)-3-[(4R,2E)-5-tert-butyldiphenylsilyloxy-4-methyl-2-pentenoyl]-4-phenyloxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / imidazole / dimethylformamide / 20 h / 20 °C

2: 93 percent / DIBAL-H / toluene; diethyl ether / 1.25 h / -80 °C

3: 70 percent / (i-Pr)2NEt; LiCl / acetonitrile / 24 h / 20 °C

With 1H-imidazole; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; lithium chloride; In diethyl ether; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1002/ejoc.200600154