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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177278Generated: November 2, 2026

18-Crown-6 → Ethyl 3-chloro-5-(2-methylphenyl)-1,2-thiazole-4-carboxylate

https://huagongshe.com/reaction/2177278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
ReactantPotassium FluorideHCID 522689—
Reactant2-Methylphenyl boronic acidHCID 2733267—
ReactantEthyl 3,5-dichloro-1,2-thiazole-4-carboxylateHCID 90418456—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-chloro-5-(2-methylphenyl)-1,2-thiazole-4-carboxylateHCID 90418344—

Reaction Conditions

Temperature110 °C

Reaction Steps

Into a 100-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed ethyl 3,5-dichloro-1,2-thiazole-4-carboxylate (1 g, 4.42 mmol, 1.00 equiv), (2-methylphenyl)boronic acid (665 mg, 4.89 mmol, 1.11 equiv), Pd(OAc)2 (49.7 mg, 0.22 mmol, 0.05 equiv), KF (773 mg), 18-Crown-6 (117 mg, 0.44 mmol, 0.10 equiv), Tol (40 mL). The resulting solution was stirred overnight at 110° C. in an oil bath. The resulting solution was diluted with 50 mL of EA. The resulting mixture was washed with 5×30 mL of sodium chloride(aq). The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (0:100). This resulted in 730 mg (59%) of ethyl 3-chloro-5-(2-methylphenyl)-1,2-thiazole-4-carboxylate as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-26e8cee276a44041ae62f50243798452
Source noteuspto-grants-2015_06