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
In 20 ml of dichloromethane was suspended 1.00 g of 3-bromo-2-oxoglutaric acid. To the suspension was added 0.33 ml of ethane thiol under ice-cooling and stirring, to which was added 1.83 ml of triethylamine. The reaction solution was stirred at room temperature for 3 hours, then the solvent was evaporated off. The residue was shaken with a mixture of ethyl acetate and 1N-HCl. The ethyl acetate layer was taken, washed with water and dried (Na2SO4). The solvent was evaporated off to give 0.82 g of 3-ethylthio-2-oxoglutaric acid as pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04851422 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-def02507baea4e32b7f811a31270ba82 |
| Source note | uspto-grants-1989_07 |