(R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

Base Information

Chemical Name:(R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one
CAS No.:637337-46-3
Molecular Formula:C₄₃H₄₅NO₄Si
Molecular Weight:667.92
Hs Code.:

Synonyms:(R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

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Chemical Property of (R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

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Technology Process of (R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

There total 3 articles about (R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-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: 79.0%

: 191090-32-1
(R)-4-(1-methylethyl)-5,5-diphenyl-1,3-oxazolidin-2-one

: 671233-59-3
3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}propanoic acid

: 637337-46-3
(R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

Guidance literature:: 3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}propanoic acid; With pivaloyl chloride; triethylamine; In tetrahydrofuran; at -30 ℃; for 1.5h;

(R)-4-(1-methylethyl)-5,5-diphenyl-1,3-oxazolidin-2-one; With lithium chloride; In tetrahydrofuran; at -30 - 25 ℃;
DOI:10.1002/hlca.200390337

Reference yield:

: 501-97-3
4-hydroxyphenylpropionic acid

: 637337-46-3
(R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: 77 percent / 1H-imidazole / dimethylformamide / 5 h / 25 °C

2.1: pivaloyl chloride; Et₃N / tetrahydrofuran / 1.5 h / -30 °C

2.2: 79 percent / LiCl / tetrahydrofuran / -30 - 25 °C

With 1H-imidazole; pivaloyl chloride; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1002/hlca.200390337

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 637337-46-3
(R)-3-(3-{4-[(tert-butyldiphenylsilyl)oxy]phenyl}-1-oxopropyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: 77 percent / 1H-imidazole / dimethylformamide / 5 h / 25 °C

2.1: pivaloyl chloride; Et₃N / tetrahydrofuran / 1.5 h / -30 °C

2.2: 79 percent / LiCl / tetrahydrofuran / -30 - 25 °C

With 1H-imidazole; pivaloyl chloride; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1002/hlca.200390337