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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254400Generated: November 2, 2026

Sodium borohydride → HCID 19744527, compound

https://huagongshe.com/reaction/2254400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19744731HCID 19744731—
SolventEthanolHCID 702—
ProductHCID 19744527HCID 1974452746.8%

Reaction Steps

85 mg of the (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methyl-3-(3-formylbenzyloxy)benzylamine obtained as above was dissolved in 2 ml of ethanol, and under ice cooling, 8.6 mg of sodium borohydride was added with stirring for 30 minutes. The solvent was evaporated under reduced pressure. The residue was dissolved in a mixture of ethyl acetate and water. The organic layer was separated, and dried over anhydrous magnesium sulfate. The desiccant was removed by filtration, and the solvent was evaporated. The residue was purified by silica gel column chromatography (Wakogel C-200, 15 g; eluting solvent: hexane/ethyl acetate=10/1→5/1) to give 40 mg (yield 39%) of the captioned compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234946
Source datasetuspto-grants-1993_08
ORD IDord-8852bf693da548d6bf8ef4d2cc0b614a
Source noteuspto-grants-1993_08