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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975170Generated: October 29, 2026

Sodium borohydride → HCID 19970847, compound

https://huagongshe.com/reaction/975170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15442751HCID 15442751—
SolventEthanolHCID 702—
ProductHCID 19970847HCID 1997084742.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607955
Source datasetuspto-grants-1997_03
ORD IDord-575b95363d7849dfbf089ed1a00e5bb0
Source noteuspto-grants-1997_03