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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557056Generated: October 31, 2026

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

https://huagongshe.com/reaction/557056

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 numberUS08058287B2
Source datasetuspto-grants-2011_11
ORD IDord-510b5c69741d4978a547f956c8cc9052
Source noteuspto-grants-2011_11