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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050710Generated: October 26, 2026

Ethylamine → N-((2-Chlorothiazol-5-yl)methyl)ethanamine

https://huagongshe.com/reaction/1050710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-chloromethylthiazoleHCID 2763179—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventChloroformHCID 6212—
ProductN-((2-Chlorothiazol-5-yl)methyl)ethanamineHCID 22450338—

Reaction Steps

A 60˜70% aqueous solution of ethylamine (3.6 mL) and a 20% aqueous NaOH solution (8.0 mL) were added dropwise respectively into a solution of 2-chloro-5-chloromethylthiazole (3.40 g) in chloroform (40 mL), then benzyl triethyl ammonium chloride (0.1 g) was added. After stirring overnight at room temperature, the pH of the resulting mixture was adjusted to weak alkaline. The organic layer was separated while the aqueous layer was extracted with dichloromethane twice. The organic phases were combined, and dried over anhydrous sodium sulfate after washed with an iced aqueous sodium chloride solution twice, then remove the solvent under reduced pressure to obtain 2-chloro-5-ethylaminomethylthiazole 3.37 g as an oil in 95.2% purity. GC-MS: (M+) (EI, 70 eV, m/z) calc: 176. found: 176.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09386769B2
Source datasetuspto-grants-2016_07
ORD IDord-c9d488a28e0f477f8546e96f6b97a188
Source noteuspto-grants-2016_07