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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415153Generated: November 3, 2026

Benzyl chloroformate → Benzyl 2-(4-bromo-3-fluorophenyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/415153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-Bromo-3-fluorophenyl)pyrrolidineHCID 53403624—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductBenzyl 2-(4-bromo-3-fluorophenyl)pyrrolidine-1-carboxylateHCID 6662087382%

Reaction Steps

2-(4-Bromo-3-fluorophenyl)pyrrolidine (12.5 g, 51.4 mmol) was dissolved in a mixture of dioxane (180 mL) and water (120 mL) and treated with potassium carbonate (28.4 g, 0.21 mol) and benzyl chloroformate (9.65 g, 56.5 mmol) at ambient temperature overnight. The mixture was partitioned between ethyl acetate and brine. The organic phase was concentrated and the residue was purified by flash chromatography on silica gel using a gradient of 5-20% ethyl acetate in petroleum ether to give benzyl 2-(4-bromo-3-fluorophenyl)pyrrolidine-1-carboxylate as a yellow solid (15.3 g, yield 82%). LC-MS (ESI) m/z: 378 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-db67a18a4bc049eeaf20bf5f28878f7e
Source noteuspto-grants-2012_01