HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-(1H-indol-3-yl)ethane-1-thiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Thiosulfuric acid S-[2-(1H-indol-3-yl)-ethyl]ester | HCID 12255474 | — |
| Solvent | Phosphoric Acid | HCID 1004 | — |
| Product | 2-(1H-indol-3-yl)ethane-1-thiol | HCID 12244279 | — |
Reaction Steps
Thiosulfuric acid S-[2-(1H-indol-3-yl)-ethyl]ester, O-sodium salt (5.04 g, 18 mmol) was suspended in 105 ml of 50% phosphoric acid and covered with a layer of 160 ml of ether. The mixture was refluxed for 6 hours. After cooling, the phases were separated and the aqueous phase was extracted with ether and the organic phases were concentrated to dryness by evaporation. The crude product was obtained in a yield of 3.2 g (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776848B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-9cdd961442fd4204a99de19222bc8455 |
| Source note | uspto-grants-2010_08 |