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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834049Generated: October 29, 2026

Triethylamine → HCID 54376218, compound

https://huagongshe.com/reaction/1834049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-2-(diethylamine)ethane hydrochlorideHCID 13363—
ReactantHCID 20330199HCID 20330199—
SolventDimethylformamideHCID 6228—
ProductHCID 54376218HCID 54376218—

Reaction Steps

A mixture of 14.2 g (0.05 mole) of 2-nitro-3-phenyl-7-benzofurancarboxylic acid, 8.6 g (0.05 mole) of N,N-diethylamino-2-chloroethane hydrochloride, 10.1 g (0.1 mole) of triethylamine and 75 ml of N,N-dimethylformamide is heated at 90° to 100° C. for 16 hours, then left standing at 23° C. for 2 days. The mixture is cooled with an ice bath, then filtered to remove the white solid by-product. The filtrate is dissolved in diethyl ether, washed thrice with water and twice with saturated sodium chloride solution and dried. The solution is evaporated to provide an oil, N,N-diethylaminoethyl 2-nitro-3-phenyl-7-benzofurancarboxylate. This oil is dissolved in diethyl ether and treated with 25 ml of 4N-hydrochloric acid in isopropanol to provide a product which gradually solidifies. The product is recrystallized twice from ethanol to provide N,N-diethylaminoethyl 2-nitro-3-phenyl-7-benzofurancarboxylate hydrochloride, m.p. 194.5°-195° C., as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067993
Source datasetuspto-grants-1978_01
ORD IDord-8f388f4c5b884c87a7bb685536a4feda
Source noteuspto-grants-1978_01