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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834733Generated: October 25, 2026

Methanesulfonyl chloride → N-(3-bromopropyl)methanesulfonamide

https://huagongshe.com/reaction/1834733

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 numberUS04071352
Source datasetuspto-grants-1978_01
ORD IDord-4a1e12019c574a9faee2f8456737f8b6
Source noteuspto-grants-1978_01