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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710778Generated: November 1, 2026

Dichloromethane → 2-[4-(3-Chloropropoxy)phenyl]-1,3-thiazole

https://huagongshe.com/reaction/1710778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,3-Dichloro-1-ethoxy-propaneHCID 55301430—
Reactant4-(3-Chloropropoxy)benzenecarbothioamideHCID 59457462—
SolventEthanolHCID 702—
Product2-[4-(3-Chloropropoxy)phenyl]-1,3-thiazoleHCID 5425139336%

Reaction Conditions

Temperature110 °C

Reaction Steps

A solution of 4-(3-chloropropoxy)benzenecarbothioamide ax71 (0.3 g, 1 eq, 1.31 mmol) in ethyl alcohol (5 ml) is treated with 1,3-dichloro-1-ethoxy-propane (0.4 ml, 2.7 eq, 3.6 mmol) and the mixture is stirred at 110° C. during 4 h. The mixture is then poured into dichloromethane (10 ml) and is washed with water. The organic phase is dried over magnesium sulfate and concentrated. Purification by chromatography over silicagel (eluent: dichloromethane) affords 120 mg of 2-[4-(3-chloropropoxy)phenyl]-1,3-thiazole i88.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790720B2
Source datasetuspto-grants-2010_09
ORD IDord-1a190a4eb9f544a9920a3b63f89ab882
Source noteuspto-grants-2010_09