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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589347Generated: October 25, 2026

Hydrogen Bromide → N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromide

https://huagongshe.com/reaction/1589347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantN-(4-(4-(Ethylheptylamino)butyl)phenyl)methanesulfonamideHCID 9864094—
SolventDiethyl EtherHCID 3283—
ProductN-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromideHCID 7038771037%

Reaction Steps

N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide (5.56 g, 0.015 mol), prepared according to the general procedure outlined in Example 1, was dissolved in diethyl ether. The solution was cooled with a dry ice/acetone bath and diethyl ether saturated with hydrogen bromide gas was added thereto. The volatiles were evaporated under reduced pressure and 100 ml of ethyl acetate was added to the residue. The solution was triturated and appoximately 6 grams of crystals were collected. The solid was recrystallized from isopropyl alcohol to provide 2.5 g of N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromide. mp=98°-100° C. Yield 37%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04569801
Source datasetuspto-grants-1986_02
ORD IDord-6d749e6c337e414abdd3df98d3452654
Source noteuspto-grants-1986_02