HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-chloroacetoacetate → Methyl 4-methyl-2-phenyl-1,3-thiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-chloroacetoacetate | HCID 107332 | — |
| Reactant | Thiobenzamide | HCID 683563 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 4-methyl-2-phenyl-1,3-thiazole-5-carboxylate | HCID 15832490 | 42% |
Reaction Steps
A solution of methyl 2-chloroacetoacetate (1.86 g, 12.4 mmol) and thiobenzamide (1.7 g, 12.4 mmol) in EtOH (50 mL) was refluxed for 18 h. The mixture was evaporated to dryness and the resulting oil was purified by flash chromatography to give methyl 4-methyl-2-phenylthiazole-5-carboxylate (1.21 g, 42%) as a colourless oil: 1H NMR (300 MHz, CDCl3) δ (TMS) 8.0-7.9 (m, 2H, arom), 7.5-7.4 (m, 3H, arom), 3.87 (s, 3H, OMe), 2.76 (s, 3H, Me-thiazole). Analysis calculated for C12H11NO2S: C 61.78; H 4.75; N 6.00; S 13.74. Found: C 61.56; H 4.71; N 5.82; S 14.61.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05888941 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-8880208697de406abddf0784ed08c305 |
| Source note | uspto-grants-1999_03 |