Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176347Generated: October 29, 2026

Benzoyl chloride → N-Propylbenzamide

https://huagongshe.com/reaction/2176347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantPropylamineHCID 7852—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
SolventChloroformHCID 6212—
ProductN-PropylbenzamideHCID 2535492%

Reaction Steps

First, 10 g of propylamine, 26 g of triethylamine, and 200 mL of tetrahydrofuran (THF) were put in a 500 mL three-neck flask, and stirred. This mixed solution was cooled in ice, and a mixed solution of 24 g of benzoyl chloride and 50 mL of THF was dripped, and then, the temperature was increased to room temperature and the mixture was stirred for 2 hours. After the stirring, chloroform was added to this mixture, the mixture was washed with water and then a saturated aqueous solution of sodium hydrogen carbonate, and anhydrate magnesium sulfate was added for drying. The mixture after the drying was subjected to gravity filtration, and the filtrate was concentrated to give a solid. This solid was washed with hexane, so that 25 g of N-propylbenzamide was prepared as a white solid with a yield of 92%. The synthetic scheme of Step 1 is shown by (a-15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09065061B2
Source datasetuspto-grants-2015_06
ORD IDord-2fdccabe2e9c49ffa8046c700f387b4f
Source noteuspto-grants-2015_06