HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-chloroacetoacetate → Ethyl {2-[4-(trifluoromethyl)anilino]-1,3-thiazol-4-yl}acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Reactant | N-[4-(Trifluoromethyl)phenyl]thiourea | HCID 2777727 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl {2-[4-(trifluoromethyl)anilino]-1,3-thiazol-4-yl}acetate | HCID 58795531 | — |
Reaction Steps
4-Chloro-3-oxo-butyric acid ethyl ester was added to a suspension of (4-trifluoromethyl-phenyl)-thiourea (3 grams), obtained in step (ii), in ethanol (20 mL) and refluxed for about 12 hrs. The reaction mixture was cooled and the solid obtained was filtered and dried to give the pure product (4.1 grams).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08080668B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-3db1d3ef2b8b4cb7978fe0e8af6b10ec |
| Source note | uspto-grants-2011_12 |