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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903672Generated: October 26, 2026

2,4-Dichlorophenol → Ethyl 2-(2',4'-dichlorophenoxy)-4-methyl-5-thiazolecarboxylate

https://huagongshe.com/reaction/1903672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorophenolHCID 8449—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-chloro-4-methyl-1,3-thiazole-5-carboxylateHCID 594903—
SolventAcetoneHCID 180—
ProductEthyl 2-(2',4'-dichlorophenoxy)-4-methyl-5-thiazolecarboxylateHCID 1328276258.2%

Reaction Steps

A mixture of 6.24 g (0.03 mole) of ethyl 2-chloro-4-methyl-5-thiazolecarboxylate, 4.89 g (0.03 mole) of 2,4-dichlorophenol, 4.14 g (0.03 mole) of potassium carbonate and 40 ml. of acetone was held at reflux for 89 hours. Acetone was removed under reduced pressure. The residue was treated with 50 ml. of water and extracted with ether. The ether solution was washed successively with saturated sodium bicarbonate, 30 ml. of 10% sodium hydroxide and 50 ml. of water. The ether solution was dried (MgSO4) and concentrated. The residue was recrystallized from hexane to give 5.8 g (58%) of ethyl 2-(2',4'-dichlorophenoxy)-4-methyl-5-thiazolecarboxylate as a white solid, m.p. 71°-73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04437875
Source datasetuspto-grants-1984_03
ORD IDord-2243fe9876384b91917571d19f4b5926
Source noteuspto-grants-1984_03