HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414224Generated: October 30, 2026
Lawesson's reagent → HCID 14424279, compound
https://huagongshe.com/reaction/414224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 14424278 | HCID 14424278 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14424279 | HCID 14424279 | 53.9% |
Reaction Steps
To a stirred suspension of Lawesson's Reagent (2.3 g, 0.0057 mole) in approximately 40 ml of toluene was added a mixture of N-[2-(5-methylthienyl)-2-oxoethyl]-4-trifluoromethylbenzamide (3.0 g, 0.011 mole) in toluene (35 ml). After complete addition the reaction mixture was heated at reflux for approximately four hours, then was allowed to cool to room temperature and stirred for two days. The solvent was removed from the reaction mixture by evaporation under reduced pressure, leaving an oil. The oil was dissolved in a small amount of methylene chloride and purified by column chromatography on silica gel, eluting with methylene chloride, yielding 1.0 g of 5-(5-methylthien-2-yl)-2-(4-trifluoromethylphenyl)thiazole as a solid, m.p. 150°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04791124 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-ef927fe9fdb84ec9ba860d24af4838be |
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| Source note | uspto-grants-1988_12 |
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