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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873524Generated: October 26, 2026

Ammonia → (2S,4R)-1-Boc-2-carbamoyl-4-hydroxypyrrolidine

https://huagongshe.com/reaction/1873524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantAmmonium ChlorideHCID 25517—
Reactant(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acidHCID 88804—
SolventTetrahydrofuranHCID 8028—
Product(2S,4R)-1-Boc-2-carbamoyl-4-hydroxypyrrolidineHCID 1479664886%

Reaction Conditions

Temperature-15 °C

Reaction Steps

(2S,4R)-1-(tert-Butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid 13b (86.4 g, 0.374 mol) was dissolved in 1.2 L of tetrahydrofuran followed by addition of triethylamine (41 g, 0.411 mol) under argon atmosphere. The reaction mixture was cooled to −15° C., ethyl chlorformate (43.84 g, 0.411 mol) was added. After the mixture was stirred for 10 minutes, aqueous ammonia (236.8 mL) was added. The reaction mixture was slowly warmed up to 5° C. during 2 hours followed by addition of ammonium chloride (32 g). The reaction mixture was stirred for 30 minutes and separated. The separated organic phase was dried over anhydrous sodium sulfate, and the aqueous phase was extracted with ethyl acetate (100 mL×2). The combined organic extracts were concentrated under reduced pressure to obtain the title compound (2S,4R)-tert-butyl 2-carbamoyl-4-hydroxypyrrolidine-1-carboxylate 13c (74 g, yield 86%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304411B2
Source datasetuspto-grants-2012_11
ORD IDord-056d2b9a01e04737914c2b5a8787633d
Source noteuspto-grants-2012_11