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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931886Generated: October 25, 2026

Ammonium Chloride → 1-Benzyl-3-(2,3-difluorophenyl)pyrrolidin-3-ol

https://huagongshe.com/reaction/1931886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Benzyl-3-pyrrolidinoneHCID 69890—
Reactant1-Bromo-2,3-difluorobenzeneHCID 2733260—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product1-Benzyl-3-(2,3-difluorophenyl)pyrrolidin-3-olHCID 6851584957.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-bromo-2,3-difluorobenzene (25 g, 129.5 mmol) in dry diethyl ether (150 mL), under nitrogen at −78° C. was added drop wise n-butyllithium (2.5 M in hexane, 51.8 mL, 129.5 mmol). The mixture was stirred for 30 min after which a solution of 1-benzylpyrrolidin-3-one (20.4 g, 116.5 mmol) in dry diethyl ether (50 mL) was added drop wise. The mixture was stirred at −78° C. for 30 min and for 2 h at ambient temperature. Aqueous saturated ammonium chloride solution (50 mL) was added and the mixture was extracted with ethyl acetate (2×50 mL). The combined organic phase was dried (Na2SO4), filtered and evaporated. Purification by flash chromatography on silica gel (isooctane/ethyl acetate/triethyl amine, 75:20:5) gave the title compound (19.5 g). MS m/z (relative intensity, 70 eV) 289 (M+, 20), 198 (69), 133 (72), 132 (51), 91 (bp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188301B2
Source datasetuspto-grants-2012_05
ORD IDord-f4a3e1d074624c32b30b650cff58fd11
Source noteuspto-grants-2012_05