HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → 3-Ethylthio-2-oxoglutaric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromo-2-ketoglutarate | HCID 195934 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Ethylthio-2-oxoglutaric acid | HCID 15097813 | — |
Reaction Steps
To a suspension of 1.00 g of 3-bromo-2-oxoglutaric acid in 20 ml of dichloromethane was added 0.33 ml of ethane thiol while stirring under ice-cooling, followed by addition of 1.83 ml of triehtylamine. The reaction mixture was stirred at room temperature for 3 hours, then the solvent was distilled off. The residue was distributed to ethyl acetate and 1N-HCl. The ethyl acetate layer was separated, washed with water and dried (Na2SO4), followed by distilling off the solvent to give 0.82 g of 3-ethylthio-2-oxoglutaric acid as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04956358 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-5112f01feebd41dbbb44b92546e86d58 |
| Source note | uspto-grants-1990_09 |