(S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic acid tert-butyl ester
CAS No.:752244-60-3
Molecular Formula:C₁₈H₂₀F₅NO₃
Molecular Weight:393.354
Hs Code.:

Synonyms:(S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic acid tert-butyl ester

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Chemical Property of (S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic acid tert-butyl ester

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Technology Process of (S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic acid tert-butyl ester

There total 1 articles about (S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic 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: 92.0%

: 95715-87-0
(R)-3-tert-butoxycarbonyl-4-formyl-2,2-dimethyloxazolidine

: 1765-40-8
(bromomethyl)pentafluorobenzene

: 752244-60-3
(S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic acid tert-butyl ester

Guidance literature:: (bromomethyl)pentafluorobenzene; With triphenylphosphine; In tetrahydrofuran; for 0.25h;

With potassium tert-butylate; In tetrahydrofuran; at 0 ℃; for 1.5h;

(R)-3-tert-butoxycarbonyl-4-formyl-2,2-dimethyloxazolidine; In tetrahydrofuran; at -78 - 20 ℃; for 14h;
DOI:10.1021/jo049206z

Reference yield:

: 752244-60-3
(S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic acid tert-butyl ester

: (E)-(S)-2-Amino-4-pentafluorophenyl-but-3-en-1-ol

Guidance literature:: With acetyl chloride; In methanol; at 0 ℃; for 0.5h;
DOI:10.1021/jo049206z

Reference yield:

: 752244-60-3
(S)-2,2-Dimethyl-4-((E)-2-pentafluorophenyl-vinyl)-oxazolidine-3-carboxylic acid tert-butyl ester

: 752244-63-6
(S)-2-(tert-butoxycarbonyl)amino-4-(perfluorophenyl)butanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: acetyl chloride / methanol / 0.5 h / 0 °C

2: triethylamine / CH₂Cl₂ / 3 h / 20 °C

3: 98 percent / H₂ / Pd-black / ethanol / 12 h / 20 °C / atmospheric pressure

4: 64 percent / pyridinium dichromate / dimethylformamide / 20 °C

With dipyridinium dichromate; hydrogen; triethylamine; acetyl chloride; palladium; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo049206z