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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054606Generated: November 2, 2026

Triethylamine → 3-(4-Bromophenyl)-1-(methylsulfonyl)pyrrolidine

https://huagongshe.com/reaction/1054606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(4-Bromophenyl)pyrrolidine hydrochlorideHCID 53407708—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Bromophenyl)-1-(methylsulfonyl)pyrrolidineHCID 84214909108.1%

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 at room temperature for 5 minutes and treated with methanesulfonyl chloride (100 mg, 0.84 mmol). After the reaction mixture was stirred at room temperature for 20 hours, the mixture was diluted with water and extracted with EtOAc (2×20 mL). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated in vacuo to give 3-(4-bromophenyl)-1-(methylsulfonyl)pyrrolidine (0.25 g, quantitative yield) as a solid which was used for next step directly. MS (ES+) 303.9, 305.9 (79Br M+H, 81Br M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-7b9b9f6faf454e98898b1edb7f26ea18
Source noteuspto-grants-2016_07