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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242664Generated: October 31, 2026

Trifluoroacetic acid → (R)-3-(4-chloro-benzyloxy)-pyrrolidine

https://huagongshe.com/reaction/242664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(R)-3-(4-chlorobenzyloxy)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66757611—
SolventDichloromethaneHCID 6344—
Product(R)-3-(4-chloro-benzyloxy)-pyrrolidineHCID 53765332—

Reaction Steps

A solution of (R)-3-(4-chlorobenzyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.88 mmol) in dichloromethane cooled at 0° C. was treated with trifluoroacetic acid (20%) and warmed to room temperature and stirred for 2 h. The reaction mixture was concentrated in vacuo, diluted with ethyl acetate and free based with 10% aqueous sodium bicarbonate. The combined organics were dried over sodium sulfate. The product was used without any further purification. ESI-MS m/z: 211(M+1), UV retention time: 0.97 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-c617bb12dd094e24bd4854097b8c3054
Source noteuspto-grants-2014_02