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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713653Generated: October 26, 2026

Chloroacetaldehyde → (4-Methoxy-phenyl)thiazol-2-yl-amine

https://huagongshe.com/reaction/1713653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant4-ThioureidoanisoleHCID 667549—
SolventEthanolHCID 702—
Product(4-Methoxy-phenyl)thiazol-2-yl-amineHCID 956680—

Reaction Steps

A mixture of (4-methoxy-phenyl)-thiourea (3.0 g, 16.5 mmol) and a 45% aqueous solution of chloroacetaldehyde (12 mL, 82.4 mmol, 5.0 equiv) in EtOH (23 mL) is heated to reflux for 1 h. The resulting dark orange solution is allowed to cool to RT and concentrated in vacuo. NaHCO3 is then added to the oily residue until CO2 evolution subsides and a beige precipitate forms. The product is collected by vacuum filtration, washed thoroughly with water (600 mL), and dried in vacuo. Title compound: ES-MS: 207.0 [M+H]+; single peak at tR=5.32 min (System 1); Rf=0.17 (CH2Cl2/MeOH, 95/5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795288B2
Source datasetuspto-grants-2010_09
ORD IDord-73cbf53bae11469aa911c9e263bd879e
Source noteuspto-grants-2010_09