HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781588Generated: October 26, 2026
Ethyl (chloroformyl)acetate → Ethyl 2-(trifluoromethyl)-1,3-thiazole-5-carboxylate
https://huagongshe.com/reaction/1781588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl (chloroformyl)acetate | HCID 118030 | — |
| Reactant | Trifluoroethanethioamide | HCID 4425751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(trifluoromethyl)-1,3-thiazole-5-carboxylate | HCID 15171126 | 24.7% |
Reaction Steps
A mixture of 11.22 g of 2,2,2,-trifluorothioacetamide and 10.14 g of ethyl 2-chloro-2-formylacetate was stirred for 30 minutes in an oil bath of 70° C. and then for 1.5 hours in an oil bath of 100° C., to which 100 ml of dichloromethane were added. After removing an insoluble substance, the mixture was concentrated and the residue was subjected to a column chromatography [developing solvent: hexane-ethyl acetate (10:1)], to obtain 3.74 g of ethyl 2-(trifluoromethyl)-5-thiazolecarboxylate as yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05633375 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-e77115f6fff944f5b5d1ed887385f92e |
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| Source note | uspto-grants-1997_05 |
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