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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260664Generated: October 31, 2026

Sodium borohydride → HCID 19970847, compound

https://huagongshe.com/reaction/2260664

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 ml 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 numberUS05478840
Source datasetuspto-grants-1995_12
ORD IDord-0f6e1fc5765c4e0c93e22d31c00daa01
Source noteuspto-grants-1995_12