HuagongsheHuagongshe Chemistry Print Report · For research reference only
(E)-(6-methoxy-2-phenylindan-1-ylidene)acetonitrile → 2-(6-Methoxy-2-phenylindan-1-ylidene)ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (E)-(6-methoxy-2-phenylindan-1-ylidene)acetonitrile | HCID 10858248 | — |
| Reactant | Ethanol, reaction products with ammonia, distn. residues | HCID 22020343 | — |
| Catalyst | Cobalt | HCID 104730 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(6-Methoxy-2-phenylindan-1-ylidene)ethylamine | HCID 57055373 | — |
Reaction Steps
To a solution of (E)-(6-methoxy-2-phenylindan-1-ylidene)acetonitrile (0.45 g, 1.72 mmol.) in ethanol (30 ml) were added a saturated ammonia/ethanol solution (10 ml) and Raney cobalt (0.3 g). The mixture was stirred for 10 hours at 10 hours at room temperature under hydrogen atmosphere (5 kgf/cm2). The Raney cobalt was filtered off, then the solvent was filtered off under reduced pressure to leave 2-(6-methoxy-2-phenylindan-1-ylidene)ethylamine., which was dissolved in a hydrogen chloride/ethanol solution. The solvent was then distilled off under reduced pressure to afford the titled compound (0.3 g, yield 58%). This compound was used for the subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05922771 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-d11e4db540cc4e86aeae124281e2527a |
| Source note | uspto-grants-1999_07 |