HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium ethanethioate → HCID 131735876, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | HCID 90238121 | HCID 90238121 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131735876 | HCID 131735876 | — |
Reaction Steps
(2S)-1-(3,5-bis(trifluoromethyl)phenyl)-2-((tert-butoxycarbonyl)amino)propyl methanesulfonate (1.0 g, 2.15 mmol) and potassium ethanethioate (0.736 g, 6.45 mmol) were combined in DMF (5 ml). The reaction was stirred at room temperature for 5 hours under a N2 atmosphere. The reaction was diluted with 30% EtOAc in hexane, washed with water, then brine, dried over Na2SO4, filtered and concentrated. The compound was purified by column chromatography to yield S-((2S)-1-(3,5-bis(trifluoromethyl)phenyl)-2-((tert-butoxycarbonyl)amino)propyl) ethanethioate. 1H NMR (500 MHz, CDCl3): δ 7.84 (s, 2H); 7.79 (s, 1H); 4.91 (s, 1H); 4.51 (s, 1H); 4.21 (s, 1H); 2.40 (s, 3H); 1.38 (s, 9H); 1.19 (d, J=6.9 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09376408B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-f8d3b17432a8421ead16ff86d8444227 |
| Source note | uspto-grants-2016_06 |