HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 67185016, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 67187925 | HCID 67187925 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67185016 | HCID 67185016 | — |
Reaction Steps
(1,4-Dimethyl-1H-indol-3-yl)-acetonitrile (6.0 g, 33 mmol) is suspended in ethanol (150 mL) and then potassium hydroxide (10.6 g, 162 mmol) in water (150 mL) is added to the solution. The reaction is stirred and then heated to reflux for 16 hours. the reaction is then cooled to room temperature and diluted with water. The aqueous layer is washed with DCM (3×150 mL) and then the water layer is cooled to zero and acidified with the addition of 12N HCl. The resulting suspension is extracted with DCM (3×100 mL) and the organic layers are combined, filtered and evaporated in vacuo. The resulting product is used without further purification (3.9 g, 20 mmol, 60%) LC/MS (M++1): 204.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969348B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-1a5f877132aa4a43b096dd22a1be286e |
| Source note | uspto-grants-2015_03 |