HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-chloroacetoacetate → Ethyl 2-ethyl-4-methyl-1,3-thiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | Propanethioamide | HCID 2760628 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-ethyl-4-methyl-1,3-thiazole-5-carboxylate | HCID 23560693 | 81.5% |
Reaction Steps
A solution of ethyl 2-chloroacetoacetate (2.00 g, 10.04 mmol) and thiopropionamide (1.00 g, 11.22 mmol) in ethanol (100 mL) was heated at reflux overnight. The solvent was evaporated and dichloromethane (100 mL) added. The solution was washed with water (2×100 mL) and brine (100 mL), dried (MgSO4), filtered, evaporated and the concentrate was chromatographed over silica gel (10% ethyl acetate/hexanes) to give 2-ethyl-4-methylthiazole-5-carboxylic acid ethyl ester (1.63 g, 81% yield) as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06515124B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-b83915895e264ac5ae4bcc8fa8f3e220 |
| Source note | uspto-grants-2003_02 |