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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649738Generated: November 3, 2026

Sodium borohydride → HCID 14373286, compound

https://huagongshe.com/reaction/1649738

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 numberUS04921862
Source datasetuspto-grants-1990_05
ORD IDord-22312b42e15b42aca91bb1878d48182b
Source noteuspto-grants-1990_05