HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281237Generated: October 28, 2026
Ethyl 4-chloroacetoacetate → HCID 12953391, compound
https://huagongshe.com/reaction/2281237
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Reactant | 4-Fluorothiobenzamide | HCID 737223 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12953391 | HCID 12953391 | — |
Reaction Steps
To a stirred solution of 4-fluorothiobenzamide (8.94 g, 57.6 mmol) in ethanol (70 mL) was added ethyl 4-chloroacetoacetate (7.8 mL, 58 mmol). The reaction was heated at reflux for 4 hours, treated with an addition aliquot of ethyl 4-chloroacetoacetate (1.0 mL, 7.4 mmol) and refluxed for an additional 3.5 hours. The reaction was then concentrated and the residue was partitioned between ethyl acetate (200 mL) and aqueous NaHCO3 (200 mL). The organic layer was combined with a backextract of the aqueous layer (ethyl acetate, 1×75 mL), dried (Na2SO4) and concentrated. The resulting amber oil was purified by flash chromatography using a hexane/ethyl acetate gradient to afford ethyl 2-(2-(4-fluorophenyl)thiazol-4-yl)acetate as a low melting, nearly colorless solid (13.58 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139580B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-7a713490660240e598306f00f22b9861 |
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| Source note | uspto-grants-2015_09 |
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