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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158643Generated: October 30, 2026

2,2,2-Trichloroethyl chloroformate → 1-[(3SR,4RS)-4-(3,4-Dichloro-phenyl)-pyrrolidin-3-yl]-ethanone

https://huagongshe.com/reaction/1158643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
Reactant1-[(3RS,4SR)-1-Benzyl-4-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethanoneHCID 66999730—
SolventAcetonitrileHCID 6342—
Product1-[(3SR,4RS)-4-(3,4-Dichloro-phenyl)-pyrrolidin-3-yl]-ethanoneHCID 6713174863.2%

Reaction Steps

To a solution of 1-[(3SR,4RS)-1-benzyl-4-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethanone 4.00 g (9.20 mmol) dissolved in CH3CN (50 mL) was added 2.48 mL (18.40 mmol) of 2,2,2-trichloroethyl chloroformate and stirring was continued for 3 hours at RT. Volatiles were removed under vacuo, and the residue was dissolved in AcOH (30 mL) before a total of 1.5 g of Zn dust was added portion wise. After three hours at RT, the reaction mixture was filtered on celite, the solvent removed under vacuo, followed by extraction with EtOAc/aq. NaHCO3 (basic pH). The organic phases were dried on Na2SO4 and column chromatography (SiO2, CH2Cl2/MeOH 9:1 to 8:2) yielded 1.50 g (63%) of the title compound as a colorless oil. ES-MS m/e: 258.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812021B2
Source datasetuspto-grants-2010_10
ORD IDord-ef3f0cf6550c4367b0ad176540b72791
Source noteuspto-grants-2010_10