HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromopyruvate → 2-Methylpentane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 2,2-Dimethylpropanethioamide | HCID 3031130 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Methylpentane | HCID 7892 | — |
| Product | Ethyl 2-(tert-butyl)thiazole-4-carboxylate | HCID 58790291 | — |
Reaction Steps
Ethyl 3-bromo-2-oxopropanoate (6.20 mL, 49.40 mmol) was added very carefully to a stirred solution of 2,2-dimethylpropanethioamide (5.79 g, 49.40 mmol) in ethanol (60 mL). The solution was then heated under reflux for 16 h. After cooling, the reaction mixture was diluted with EtOAc, washed with saturated aqueous sodium bicarbonate solution and evaporated in vacuo. Purification by silica gel chromatography (Biotage, 100 g) eluting with EtOAc: iso-hexane, 1:10 gave the sub-title compound as a yellow oil. Yield: 6.56 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273774B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-21c25ab50d2a4c8bb9ed9ec9ca00b3dc |
| Source note | uspto-grants-2012_09 |