HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415683Generated: October 28, 2026
Triethylamine → Ethyl 2-(4-methoxyphenyl)thiazole-4-carboxylate
https://huagongshe.com/reaction/415683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 4-Methoxybenzenecarbothioamide | HCID 736827 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-(4-methoxyphenyl)thiazole-4-carboxylate | HCID 10400532 | 48.4% |
Reaction Steps
To an ice-cold solution of 4-methoxy-thiobenzamide (0.50 g, 2.98 mmol) in ethanol (25 ml) was added triethylamine (0.41 ml, 2.98 mmol) followed by dropwise addition of ethyl bromopyruvate (0.56 ml, 4.40 mmol). The reaction mixture was heated at 65° C. for 12 h. After the completion of the reaction mixture (TLC monitoring), the reaction mixture was evaporated to dryness under reduced pressure, water (25 mL) was added and extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (60-120 M, 10% EtOAc-Hexane) to get the desired product (0.38 g, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08088791B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-3024e8cd7e984977b1ba42ee5300074e |
|---|
| Source note | uspto-grants-2012_01 |
|---|