HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975170Generated: October 29, 2026
Sodium borohydride → HCID 19970847, compound
https://huagongshe.com/reaction/975170
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15442751 | HCID 15442751 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19970847 | HCID 19970847 | 42.3% |
Reaction Steps
5-Benzyl-2-formyl-10,11-dihydro-5H-dibenz[b,f]azepine (3.29 g) was dissolved in 200 m. of ethanol, and 0.5 g of sodium borohydride was added to the solution, followed by stirring at room temperature for 30 minutes. The solvent was distilled off under reduced pressure, and the residue was diluted with dichloromethane. The mixture was washed with 1N aqueous hydrochloric acid and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was dissolved in 300 ml of ethanol. To the solution was added 300 mg of 10% palladium carbon and the mixture was stirred in a stream of hydrogen for 4 days. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography [eluent: hexane/ethyl acetate (2/1)] to give 1.0 g (42%) of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607955 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-575b95363d7849dfbf089ed1a00e5bb0 |
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| Source note | uspto-grants-1997_03 |
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