HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 2-methyl-1,3-thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | Thioacetamide | HCID 2723949 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-methyl-1,3-thiazole-4-carboxylate | HCID 293353 | — |
Reaction Steps
5.00 g of ethanethioamide was suspended in 50 mL of ethanol, to which 9.3 mL of ethyl 3-bromo-2-oxopropanoate was added dropwise at room temperature, and this suspension was stirred for one hour while heating it under reflux. The reaction mixture was cooled to room temperature and added to a mixture of ethyl acetate and water, followed by separation of the organic phase therefrom. After the resultant organic phase was washed with water and a saturated sodium chloride solution successively, the washed phase was dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure to yield 2.30 g of ethyl 2-methyl-1,3-thiazole-4-carboxylate as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772285B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-3e4f7b4a41df49049212ab0dd143a4e6 |
| Source note | uspto-grants-2010_08 |