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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397183Generated: October 25, 2026

Methanesulfonyl chloride → N-(3-bromopropyl)methanesulfonamide

https://huagongshe.com/reaction/2397183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Bromopropan-1-amine hydrobromideHCID 12570703—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
ProductN-(3-bromopropyl)methanesulfonamideHCID 11218181—

Reaction Steps

To a cooled solution of 2-bromopropylamine hydrobromide (43.8 g., 0.20 mole) in pyridine (100 ml.) was added over a period of 40 minutes methanesulfonyl chloride (15.2 ml., 0.20 mole). The reaction mixture was stirred for 15 minutes and then diluted with ether. The remaining solid was filtered off, washed with about 200 ml. of acetone. The filtrate and washes were concentrated in vacuo. The residue was extracted with three 100 ml. portions of acetone. Upon evaporation of the acetone, 30.4 g. of a thick oil representing the title compound. The product was confirmed by infrared analysis and nuclear magnetic resonance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04021229
Source datasetuspto-grants-1977_05
ORD IDord-02dfdb0a437d48239751e313a39f518d
Source noteuspto-grants-1977_05