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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905285Generated: October 27, 2026

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

https://huagongshe.com/reaction/905285

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 numberUS04423051
Source datasetuspto-grants-1983_12
ORD IDord-ba8d235a86664172a970eebf47ff6812
Source noteuspto-grants-1983_12