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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461839Generated: October 29, 2026

Triethylamine → HCID 21392757, compound

https://huagongshe.com/reaction/461839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant5-Hexen-1-amineHCID 533877—
Reactant2-Ethylthio-5-carboxythiazoleHCID 21391910—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21392757HCID 21392757—

Reaction Conditions

Temperature-30 °C

Reaction Steps

In this preparation 0.1 mole of 2-ethylthio-5-carboxythiazole is dissolved in 300 ml. of anhydrous tetrahydrofuran, under nitrogen, and 0.1 mole of triethylamine is added and the resulting mixture cooled to -30° C. 0.1 Mole of ethylchloroformate is then added dropwise with stirring and the resulting mixture allowed to warm to 0° C. The mixture is then stirred for ten minutes, then cooled to -30° C and 0.11 mole of 1-aminohex-5-ene in 50 ml. of tetrahydrofuran added dropwise. The mixture is allowed to warm to room temperature (about 20° C), poured in 500 ml. of ethyl acetate, washed with water, then washed with saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture is then filtered and the resulting filtrate evaporated under vacuum yielding 2-ethylthio-5-(hex-5-enylaminocarbonyl)thiazole as a solid, which is then further purified by recrystallization from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064259
Source datasetuspto-grants-1977_12
ORD IDord-c29e0b0155fd433f99d1ce862c68aea6
Source noteuspto-grants-1977_12