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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62636Generated: October 30, 2026

Hydrochloric Acid → 1-Benzyl-3-(3,5-dichlorophenyl)-3-(trifluoromethyl)pyrrolidine

https://huagongshe.com/reaction/62636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 118270793HCID 118270793—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-3-(3,5-dichlorophenyl)-3-(trifluoromethyl)pyrrolidineHCID 5821888388.3%

Reaction Steps

1-Benzyl-3-(3,5-dichlorophenyl)-3-(trifluoromethyl)-2,3-dihydro-1H-pyrrole (100 mg, 90% purity, 242 μmol) was dissolved in tetrahydrofurane (2 mL) and sodium borohydride (26.0 mg, 677 μmol) was added at room temperature. After 30 minutes at room temperature the reaction mixture was acidified with hydrochloric acid (3.6%) and extracted twice with dichloromethane. The combined organic phases were washed with water, dried over sodium sulfate, filtered and the solvents evaporated. This procedure yielded 1-benzyl-3-(3,5-dichlorophenyl)-3-(trifluoromethyl)pyrrolidine (80.0 mg, 79% purity, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447036B2
Source datasetuspto-grants-2016_09
ORD IDord-35e6ccda475f4404b8484cb5bd581a8d
Source noteuspto-grants-2016_09