HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977984Generated: November 1, 2026
Ethanol, reaction products with ammonia, distn. residues → HCID 21996512, compound
https://huagongshe.com/reaction/1977984
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol, reaction products with ammonia, distn. residues | HCID 22020343 | — |
| Reactant | HCID 54328648 | HCID 54328648 | — |
| Catalyst | Cobalt | HCID 104730 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21996512 | HCID 21996512 | 53.7% |
Reaction Steps
To a solution of (1,2,3,4-tetrahydro-7-methoxy-1-naphthylidene)acetonitrile (4.0 g, 20 mmol) in ethanol (10 ml) were added a saturated ammonia/ethanol solution (5 ml) and Raney cobalt (ODHT-60, 1 g). The reaction mixture was stirred for 3.5 hours at room temperature under hydrogen atmosphere (about 4 kgf/cm2). The Raney cobalt was filtered off, then the solvent was distilled off under reduced pressure. To the residue was added dilute hydrochloric acid, then the organic layer was subjected to extraction with ethyl acetate. The extract solution was washed with a saturated aqueous solution of sodium hydrogencarbonate and water, which was dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was purified by means of a silica gel column chromatography to give the above-titled compound (yield 2.14 g, oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06235789B1 |
|---|
| Source dataset | uspto-grants-2001_05 |
|---|
| ORD ID | ord-31d3ae4f705a461cacd3bfd4b17bbbba |
|---|
| Source note | uspto-grants-2001_05 |
|---|