tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate

Base Information

Chemical Name:tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate
CAS No.:1260507-57-0
Molecular Formula:C₂₀H₂₆N₂O₅
Molecular Weight:374.437
Hs Code.:

Synonyms:tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate

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Chemical Property of tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate

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Technology Process of tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate

There total 6 articles about tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate 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: 66.0%

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 90719-32-7
(S)-4-Benzyl-2-oxazolidinone

: 1260507-57-0
tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 0 - 20 ℃; for 16h; Inert atmosphere;
DOI:10.1021/ol102613z

Reference yield: 48.0%

: 74108-10-4
C₆H₁₅N*C₁₀H₁₇NO₄

: 90719-32-7
(S)-4-Benzyl-2-oxazolidinone

: 75-65-0
tert-butyl alcohol

: 1260507-57-0
tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate

: 91237-84-2
N-BOC-proline tert-butyl ester

Guidance literature:: With dmap; dicyclohexyl-carbodiimide;
DOI:10.1055/s-0030-1258428

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1260507-57-0
tert-butyl (S)-2-[(S)-4-benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / tetrahydrofuran; water / 19 h / 20 °C / Cooling with ice

2: dmap; dicyclohexyl-carbodiimide / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere

With dmap; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/ol102613z