HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Phenylenediacetonitrile → 2,3,4,5-Tetrahydro-1H-benzo(d)azepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Phenylenediacetonitrile | HCID 69180 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,3,4,5-Tetrahydro-1H-benzo(d)azepine | HCID 1400243 | 35% |
Reaction Steps
1,2-Phenylenediacetonitrile (7.5 g, 48 mmol) dissolved in ethanol (150 ml) was added to Raney Ni (2 g) which had been previously washed with ethanol (3×20 ml). The mixture was then hydrogenated at 50° C. at 50 psi pressure with shaking for 24 h. The reaction mixture was then cooled to room temperature and filtered through a pad of kieselguhr and washed through with ethanol (100 ml). The filtrate was evaporated in vacuo to give a brown oil which was chromatographed on silica gel (100 g), eluting with 2-10% methanol in CH2Cl2 to give the title compound as a brown oil (2.45 g, 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429579B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-b496c791c22a479b833bb2b691e70546 |
| Source note | uspto-grants-2008_09 |