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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508316Generated: October 30, 2026

Water → 3-(3,4,5-Trichlorophenyl)-3-(trifluoromethyl)pyrrolidine

https://huagongshe.com/reaction/1508316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant1-Benzyl-3-(3,4,5-trichloro-phenyl)-3-trifluoromethyl-pyrrolidineHCID 89994601—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
Product3-(3,4,5-Trichlorophenyl)-3-(trifluoromethyl)pyrrolidineHCID 5945337292.6%

Reaction Steps

To a stirred solution of 1-benzyl-3-(3,4,5-trichloro-phenyl)-3-trifluoromethyl-pyrrolidine (Preparation 38, 4 g, 9.828 mmol) in 1,2-dichloroethane (40 mL) was added 1-chloroethyl chloroformate (1.91 mL, 17.69 mmol) and the resulting reaction mixture was refluxed for 3 hours. After complete consumption of starting material, reaction mixture was concentrated under reduced pressure to afford yellow oily residue, which was dissolved in MeOH (40 mL) and the mixture was refluxed at 2 hours. After complete consumption of starting material, reaction mixture was concentrated in vacuo to afford yellow oil, to which water (50 mL) was added and extracted with hexane (3×50 mL). Aqueous layer was basified using saturated sodium bicarbonate solution and extracted with ethyl acetate (3×50 mL). Combined organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford brown thick oil (5.5 g, crude). Crude compound was purified by column chromatography using 100-200 mesh silica gel. Desired compound was eluted in 4% methanol in dichloromethane to afford product as yellow thick oil (2.9 g, impure). Impure compound was as such for next reaction. (m/z): 317.9 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221835B2
Source datasetuspto-grants-2015_12
ORD IDord-0ae92ef5e886445eb270a65709ff99b9
Source noteuspto-grants-2015_12