HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489556Generated: October 30, 2026
Potassium ethanethioate → HCID 54193495, compound
https://huagongshe.com/reaction/1489556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | (2R,3S)-2-Bromo-3-methylpentanoic acid | HCID 51381013 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54193495 | HCID 54193495 | 81.8% |
Reaction Steps
2.11 g (10.8 mmol) of (2R,3S)-2-bromo-3-methylpentanoic acid obtained in the Synthesis Example C-1 was dissolved in 43 ml of acetonitrile and 1.42 g of potassium thioacetate was added thereto at 0° C. The mixture was stirred at0° C. for 30 minutes and then at room temperature for 5 hours. After filtering off the insoluble matters, the filtrate was concentrated. To the residue were added ether and a saturated aqueous solution of sodium hydrogencarbonate, followed by separation. The aqueous phase was acidified by adding a 2N aqueous solution of hydrochloric acid at a low temperature and then extracted with ether. The ether phase was washed with a saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and concentrated. Thus, 1.68 g of the title compound was obtained as a colorless oil (yield 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05679671 |
|---|
| Source dataset | uspto-grants-1997_10 |
|---|
| ORD ID | ord-e7a02601b1f74175b70264d97976d204 |
|---|
| Source note | uspto-grants-1997_10 |
|---|