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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910438Generated: November 1, 2026

2,2,2-Trichloroethyl chloroformate → [(3RS,4SR)-4-(3,4-Dichloro-phenyl)pyrrolidin-3-yl]-methyl-(4-trifluoromethyl-benzyl)-amine

https://huagongshe.com/reaction/910438

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
Reactant[(3RS,4SR)-1-Benzyl-4-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-methyl-(4-trifluoromethyl-benzyl)-amineHCID 67218013—
SolventAcetonitrileHCID 6342—
Product[(3RS,4SR)-4-(3,4-Dichloro-phenyl)pyrrolidin-3-yl]-methyl-(4-trifluoromethyl-benzyl)-amineHCID 6721781665.9%

Reaction Steps

To a stirred solution of [(3RS,4SR)-1-benzyl-4-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-methyl-(4-trifluoromethyl-benzyl)-amine (160 mg, 0.32 mmol) in CH3CN (5 ml) at RT, was added 2,2,2-trichloroethyl chloroformate (0.070 ml, 0.48 mmol). The reaction mixture was stirred at RT for 3 hours, concentrated under vacuo. The residue was dissolved in AcOH (3 ml) and zinc dust (80 mg) was added portion wise over 1 hours. The solvent was evaporated, the residue diluted in EtOAc and the organic phase was washed with an aqueous solution of NaHCO3. The organic phase was dried over Na2SO4 and concentrated under vacuo. The product was purified by column chromatography (CH2Cl2/MeOH: 9/1) to afford 85 mg (65%) of the tile compound as a colorless oil. ES-MS m/e: 403.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022099B2
Source datasetuspto-grants-2011_09
ORD IDord-6c61ffa6177d473da6385aff1a5b97e8
Source noteuspto-grants-2011_09