Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957350Generated: November 4, 2026

4-Phenoxybenzaldehyde → HCID 53817986, compound

https://huagongshe.com/reaction/1957350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxybenzaldehydeHCID 66139—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-Butanamine, (S)-HCID 6713753—
SolventMethanolHCID 887—
ProductHCID 53817986HCID 5381798677%

Reaction Steps

4-Phenoxybenzaldehyde (8.13 g, 41 mmol) and (S)-sec-butylamine (3 g, 41 mmol) were dissolved in methanol (137 mL) under a nitrogen at room temperature. Sodium cyanoborohydride (2.58 g) was added, and stirring was continued for 18 hours. The solvent was removed, and the residue was suspended in ether, washed with brine and dried over Na2SO4. The ether was evaporated, and the crude product was chromatographed on silica gel eluting with 3% methanol in methylene chloride to provide 7.24 g (77%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783593
Source datasetuspto-grants-1998_07
ORD IDord-4c7dad8b56bb419d98701823fa76796b
Source noteuspto-grants-1998_07