HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromopyruvate → Ethyl 2-ethyl-1,3-thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | Propanethioamide | HCID 2760628 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-ethyl-1,3-thiazole-4-carboxylate | HCID 15056276 | — |
Reaction Steps
Ethyl 3-bromo-2-oxopropanoate (4.10 mL, 32.67 mmol) was added dropwise over 10 min to a stirred solution of propanethioamide (3 g, 33.65 mmol) in ethanol (40 mL) cooled in an ice bath. After 16 h the reaction mixture was evaporated in vacuo. Purification was by silica gel chromatography eluting with EtOAc:iso-hexanes, 1:3 to give the sub-title compound as a yellow oil. Yield: 2.78 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273774B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-a2016dbc73054a85a204793783074cae |
| Source note | uspto-grants-2012_09 |