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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600908Generated: October 30, 2026

Sodium borohydride → HCID 21830758, compound

https://huagongshe.com/reaction/1600908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21830654HCID 21830654—
SolventMethanolHCID 887—
ProductHCID 21830758HCID 2183075849.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-{6-(Methoxymethoxy)-2-naphthyl}-5-(3-pyridyl)-3-pentanone (1.9 g; from Example 31 above) was immediately dissolved in methanol (100 ml) and cooled to 0° C. Solid sodium borohydride (0.284 g) was added and the reaction mixture stirred at 25° C. for 2 hours. The mixture was concentrated under reduced pressure and water was added to the residue. The aqueous mixture was extracted with ethyl acetate. The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica eluting with dichloromethane:methanol (95:5) to give an oil (0.94 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977105
Source datasetuspto-grants-1999_11
ORD IDord-0965176c03764604a506592970cbce67
Source noteuspto-grants-1999_11