Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606181Generated: November 1, 2026

Triethylamine → 2-Phenyl-5-cyclopropylcarbonyl-4,6,7,8-tetrahydrofuro[3,2-c]azepine

https://huagongshe.com/reaction/1606181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
Reactant2-Phenyl-4,6,7,8-tetrahydrofuro[3,2-c]azepineHCID 21546086—
SolventChloroformHCID 6212—
Product2-Phenyl-5-cyclopropylcarbonyl-4,6,7,8-tetrahydrofuro[3,2-c]azepineHCID 21546076—

Reaction Steps

A solution of 1.8 g. of cyclopropylcarbonyl chloride in 50 ml. of dry chloroform is added dropwise to a cooled mixture of 3.1 g. of 2-phenyl-4,6,7,8-tetrahydrofuro[3,2-c]azepine and 1.7 g. of triethylamine in 50 ml. of dry chloroform. After addition, the reaction mixture is stirred at ambient temperature for 20 hours, washed with water and dried. The chloroform is removed and the residue is triturated with n-hexane to produce a solid product. The product is recrystallized from n-hexane to give 2-phenyl-5-cyclopropylcarbonyl-4,6,7,8-tetrahydrofuro[3,2-c]azepine, m.p. 108°-110°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952025
Source datasetuspto-grants-1976_04
ORD IDord-8930b3f462814145b10615bef1f1da66
Source noteuspto-grants-1976_04