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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902823Generated: October 26, 2026

Triethylamine → 4-chloro-N-(8-quinolyl)butyramide

https://huagongshe.com/reaction/1902823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant8-AminoquinolineHCID 11359—
Reactant4-Chlorobutyryl chlorideHCID 78370—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-N-(8-quinolyl)butyramideHCID 1289854653%

Reaction Steps

A solution of 8-aminoquinoline (10 L g, 0.069 mole) and triethylamine (10 ml, 0.072 mole) in dry tetrahydrofuran (40 ml) was treated dropwise at room temperature with 4-chlorobutyryl chloride (about 0.07 mole) until the green reaction mixture turned yellow in colour. The reaction was filtered and the solids (triethylamine hydrochloride) were washed with tetrahydrofuran. The combined filtrates were concentrated by vacuum distillation, (≃15 mm Hg), filtered over alumina in methylene chloride, concentrated and recyrstallized from ether/petroleum ether affording 4-chloro-N-(8-quinolyl)butyramide. An analytical sample was prepared by recrystallization (m.p. 62°-63°), yield 53%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04366158
Source datasetuspto-grants-1982_12
ORD IDord-ddf634dbbf72471799d7274361139b10
Source noteuspto-grants-1982_12