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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903424Generated: October 25, 2026

Triethylamine → 4-[(8-cyclohexyloctyl)amino]-N-3-bromopropylbenzamide

https://huagongshe.com/reaction/903424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromopropan-1-amine hydrobromideHCID 12570703—
Reactantp-(8-Cyclohexyloctyl)aminobenzoyl chloride hydrochlorideHCID 20475769—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-[(8-cyclohexyloctyl)amino]-N-3-bromopropylbenzamideHCID 20475775—

Reaction Steps

To a slurry of 21.80 g. of 2-bromopropylamine hydrobromide in 200 ml. of glyme at 3° C. is added a solution of 23.96 g. of 4-(8-cyclohexyloctylamino)benzoyl chloride hydrochloride in 65 ml. of glyme, concurrently with 26 ml. of triethylamine diluted to 39 ml. with glyme. The solution is warmed to reflux and 0.2 g. of 4-dimethylaminopyridine is added. The solution is heated for four hours and cooled overnight. The solid is removed by filtration and the filtrate diluted with 200 ml. of water. The precipitate is collected and crystallized from cyclohexane. The solid is recrystallized from acetonitrile to yield the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04227014
Source datasetuspto-grants-1980_10
ORD IDord-8ebd1c9ca8684c6ab92b724d97ae688f
Source noteuspto-grants-1980_10