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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054600Generated: November 1, 2026

Methyl chloroformate → Methyl 3-(4-bromophenyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1054600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
Reactant3-(4-Bromophenyl)pyrrolidine hydrochlorideHCID 53407708—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(4-bromophenyl)pyrrolidine-1-carboxylateHCID 84210133111.1%

Reaction Steps

Triethylamine (192 mg, 1.9 mmol) was added to a suspension of 3-(4-bromophenyl)pyrrolidine hydrochloride (200 mg, 0.76 mmol) in anhydrous THF (5 mL). The reaction mixture was stirred for 5 minutes and treated with methyl chloroformate (0.1 g, 1.05 mmol). The reaction mixture was stirred for 16 hours at room temperature. The reaction mixture was diluted with water and extracted with EtOAc (2×15 mL). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated in vacuo to give methyl 3-(4-bromophenyl)pyrrolidine-1-carboxylate (0.24 g, quantitative yield) as an oil which was used for next step directly. MS (ES+) 283.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-284611099a764e4fa4c2cf7407cf27a0
Source noteuspto-grants-2016_07