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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34946Generated: October 27, 2026

N-(2-aminoethyl)acetamide → N-{2-[(5-bromofuran-2-yl)formamido]ethyl}acetamide

https://huagongshe.com/reaction/34946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-aminoethyl)acetamideHCID 66082—
Reactant5-Bromofuran-2-carbonyl chlorideHCID 2757011—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-{2-[(5-bromofuran-2-yl)formamido]ethyl}acetamideHCID 13800218—

Reaction Steps

A solution of 22.6 g of 5-bromo-2-furancarboxylic acid chloride in 100 ml of methylene chloride was added dropwise within 20 minutes at 0°-8° to a solution, pre-cooled to 0°, of 11.0 g of monoacetyl-ethylenediamine in 250 ml of methylene chloride and 18 ml of triethylamine. The reaction mixture was stirred at room temperature overnight, suction filtered and washed with methylene chloride. There was obtained N-(2-acetamino ethyl)-5-bromo-2-furancarboxamide as pale beige crystals, m.p. 175°-176°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764522
Source datasetuspto-grants-1988_08
ORD IDord-06adfa65536a4672ba2c77c29a74e2ea
Source noteuspto-grants-1988_08