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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414559Generated: October 30, 2026

Sodium borohydride → HCID 14373286, compound

https://huagongshe.com/reaction/414559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15123282HCID 15123282—
ReactantHCID 178418361HCID 178418361—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 14373286HCID 14373286—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 240 mg of 6-[1-hydroxy-1-phenyl(3-pyridyl)methyl]-3,4-dihydrocarbostyril in 5 ml of trifluoroacetic acid at 0° C. was added 280 mg of sodium borohydride. When hydrogen evolution ceased the mixture was stirred at 25° C. for 30 minutes, then the solvent was removed under reduced pressure. The residue was added to aqueous potassium carbonate solution and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, the solvent removed under reduced pressure and the residue chromatographed on silica gel, eluting with 3% methanol in methylene chloride to give 6-[phenyl(3-pyridyl)methyl]-3,4-dihydrocarbostyril, m.p. 95°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792561
Source datasetuspto-grants-1988_12
ORD IDord-8836d1fcc9ba400ba06586397e462cdd
Source noteuspto-grants-1988_12