HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioacetamide → Methyl 2-methyl-1,3-thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | Methyl 3-chloro-2-oxopropanoate | HCID 12530121 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-methyl-1,3-thiazole-4-carboxylate | HCID 14812829 | — |
Reaction Steps
A solution of thioacetamide (132 mmol, 1.0 eq) in MeCN (250 mL) is added to a mixture of the respective 3-chloro-2-oxo-propionic acid methyl ester derivative (132 mmol, 1.0 eq) and molecular sieves (4 Å, 12 g) in MeCN (60 mL). After stirring for 5 h the mixture is cooled in an ice-bath and the obtained precipitate is filtered off. The residue is washed with cold MeCN, dried, dissolved in MeOH (280 mL) and stirred at 50° C. for 6 h. The solvents are removed in vacuo to give the corresponding 2-methyl-thiazole-4-carboxylic acid methyl ester derivatives.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106215B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-f5dfc948f7ab40e9a206080a55578619 |
| Source note | uspto-grants-2012_01 |