HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177269Generated: October 31, 2026
18-Crown-6 → Methyl 3-chloro-5-(4-methoxyphenyl)-1,2-thiazole-4-carboxylate
https://huagongshe.com/reaction/2177269
Participants
| Role | Name | HCID | Charge |
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| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Methyl 3,5-dichloro-1,2-thiazole-4-carboxylate | HCID 90418733 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | Methyl 3-chloro-5-(4-methoxyphenyl)-1,2-thiazole-4-carboxylate | HCID 90418689 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067898B1 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-1e8969db023c402aac3f9259905b0ec9 |
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| Source note | uspto-grants-2015_06 |
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