(4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-2-one

Base Information

Chemical Name:(4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-2-one
CAS No.:695165-65-2
Molecular Formula:C₁₇H₂₃NO₂SSi
Molecular Weight:333.527
Hs Code.:

Synonyms:(4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-2-one

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Chemical Property of (4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-2-one

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Technology Process of (4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-2-one

There total 3 articles about (4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-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: 80.0%

: 180675-80-3
diethyl trimethylsilylethynyl chloro silane

: 695165-63-0
(S)-4-Hydroxy-5-methoxy-1-(2-phenylsulfanyl-ethyl)-pyrrolidin-2-one

: 695165-65-2
(4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-2-one

Guidance literature:: diethyl trimethylsilylethynyl chloro silane; (S)-4-Hydroxy-5-methoxy-1-(2-phenylsulfanyl-ethyl)-pyrrolidin-2-one; With dmap; triethylamine; In dichloromethane; at 20 ℃;

With titanium tetrachloride; at -78 ℃; Further stages.;
DOI:10.1016/j.tetlet.2004.02.097

Reference yield:

: 699-12-7
2-(phenylthio)ethanol

: 695165-65-2
(4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: Ph₃P; diisopropyl azodicarboxylate

2.1: camphor sulfonic acid / methanol

3.1: NaBH₄ / tetrahydrofuran; ethanol / 0 °C

3.2: 95 percent / p-TsOH

4.1: Et₃N; 4-DMAP / CH₂Cl₂ / 20 °C

4.2: 80 percent / TiCl₄ / -78 °C

With dmap; sodium tetrahydroborate; di-isopropyl azodicarboxylate; camphor-10-sulfonic acid; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1016/j.tetlet.2004.02.097

Reference yield:

: 695165-54-9
(S)-3-Hydroxy-1-(2-phenylsulfanyl-ethyl)-pyrrolidine-2,5-dione

: 695165-65-2
(4S,5S)-4-Hydroxy-1-(2-phenylsulfanyl-ethyl)-5-trimethylsilanylethynyl-pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: NaBH₄ / tetrahydrofuran; ethanol / 0 °C

1.2: 95 percent / p-TsOH

2.1: Et₃N; 4-DMAP / CH₂Cl₂ / 20 °C

2.2: 80 percent / TiCl₄ / -78 °C

With dmap; sodium tetrahydroborate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1016/j.tetlet.2004.02.097