HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910445Generated: October 30, 2026
2,2,2-Trichloroethyl chloroformate → [(3RS,4SR)-4-(3-chloro-phenyl)-pyrrolidin-3-yl]-methyl-(4-trifluoromethyl-benzyl)-amine
https://huagongshe.com/reaction/910445
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2,2-Trichloroethyl chloroformate | HCID 87063 | — |
| Reactant | [(3RS,4SR)-1-Benzyl-4-(3-chloro-phenyl)-pyrrolidin-3-yl]-methyl-(4-trifluoromethyl-benzyl)-amine | HCID 67218077 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [(3RS,4SR)-4-(3-chloro-phenyl)-pyrrolidin-3-yl]-methyl-(4-trifluoromethyl-benzyl)-amine | HCID 67218391 | 76% |
Reaction Steps
To a stirred solution of [(3RS,4SR)-1-benzyl-4-(3-chloro-phenyl)-pyrrolidin-3-yl]-methyl-(4-trifluoromethyl-benzyl)-amine (500 mg, 1.09 mmol) in CH3CN (7 ml) at RT, was added 2,2,2-trichloroethyl chloroformate (0.22 ml, 1.63 mmol). The reaction mixture was stirred at RT for 3 hours, concentrated under vacuo. The residue was dissolved in AcOH (5 ml) and zinc dust (200 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 305 mg (76%) of the tile compound as a colorless oil. ES-MS m/e: 369.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022099B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-994cc44420dd470c9defe7aa19e4c233 |
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| Source note | uspto-grants-2011_09 |
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