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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338263Generated: October 29, 2026

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

https://huagongshe.com/reaction/338263

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 numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-316407eb581a4b65a5117f156cf0cb44
Source noteuspto-grants-2014_11