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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177269Generated: November 1, 2026

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

https://huagongshe.com/reaction/2177269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantPotassium FluorideHCID 522689—
ReactantMethyl 3,5-dichloro-1,2-thiazole-4-carboxylateHCID 90418733—
Catalystpalladium(II) acetateHCID 167845—
ProductMethyl 3-chloro-5-(4-methoxyphenyl)-1,2-thiazole-4-carboxylateHCID 90418689—

Reaction Conditions

Temperature110 °C

Reaction Steps

Into a 25-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of methyl 3,5-dichloro-1,2-thiazole-4-carboxylate (300 mg, 1.41 mmol, 1.00 equiv) in Tol (5 mL), (4-methoxyphenyl)boronic acid (270 mg, 1.78 mmol, 1.26 equiv), Pd(OAc)2 (17 mg, 0.08 mmol, 0.05 equiv), KF (260 mg), 18-Crown-6 (180 mg, 0.68 mmol, 0.48 equiv). The resulting solution was stirred for 2 h at 110° C. in an oil bath. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:19). This resulted in 330 mg (74%) of methyl 3-chloro-5-(4-methoxyphenyl)-1,2-thiazole-4-carboxylate as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-1e8969db023c402aac3f9259905b0ec9
Source noteuspto-grants-2015_06