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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880206Generated: November 1, 2026

2,2,2-Trichloroethyl chloroformate → Ethyl 4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate

https://huagongshe.com/reaction/1880206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
ReactantEthyl 1-benzyl-4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylateHCID 67131665—
SolventAcetonitrileHCID 6342—
ProductEthyl 4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylateHCID 6732757297.1%

Reaction Steps

To a solution of (3SR,4RS)-1-benzyl-4-(3,4-dichloro-phenyl)-pyrrolidine-3-carboxylic acid ethyl ester (2.50 g, 6.61 mmol) in CH3CN (55 mL) was added 2,2,2-trichloroethyl chloroformate (1.34 mL, 9.91 mmol) and stirring was continued for 4 hours at RT. Volatiles were removed under vacuo, and the residue was dissolved in AcOH (25 mL). Then Zn dust (1.20 g) was added portion wise. After three hours at RT the reaction mixture was filtered on celite, the solvent removed under vacuo followed by an extraction with EtOAc/aq. NaHCO3 (basic pH). The organic phases were dried on Na2SO4 and column chromatography (SiO2, CH2Cl2/MeOH 9:1) yielded 1.85 g (97%) of the title compound as a light yellow oil. ES-MS m/e: 288.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318759B2
Source datasetuspto-grants-2012_11
ORD IDord-9b06aae80d294dae9aafc3afd2698dc5
Source noteuspto-grants-2012_11