HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Bromo-2-(3-pyridylmethylene)-1-tetralone → 7-Bromo-2-(3-pyridylmethyl)-1-tetralone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Bromo-2-(3-pyridylmethylene)-1-tetralone | HCID 53922358 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Bromo-2-(3-pyridylmethyl)-1-tetralone | HCID 23320898 | 85.8% |
Reaction Steps
A solution of 7-bromo-2-(3-pyridylmethylene)-1-tetralone (13.9 g) in ethanol (150 ml) containing 5% palladium on charcoal (0.50 g) was hydrogenated at 25° and 4 atm. pressure until the theoretical quantity of hydrogen had been taken up. The catalyst was filtered off and the filtrate was evaporated. The residue was distilled to give an oil (12.0 g), b.p. 200°-240° at 1.0 mm containing ca 40% of debrominated material. The product was purified by high pressure liquid chromatography using a silica gel column and a mixture of hexane and ethyl acetate (45:55) as eluent. Debrominated product was eluted first followed by pure 7-bromo-2-(3-pyridylmethyl)-1-tetralone, m.p. 63°-67°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04590200 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-c0565fa361a14ef2af64f216c89619b6 |
| Source note | uspto-grants-1986_05 |