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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957351Generated: November 2, 2026

4-Phenoxybenzaldehyde → HCID 53817987, compound

https://huagongshe.com/reaction/1957351

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxybenzaldehydeHCID 66139—
Reactant(R)-sec-butylamineHCID 2724537—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductHCID 53817987HCID 5381798777%

Reaction Steps

4-Phenoxybenzaldehyde (8.13 g, 41 mmol) and (R)-sec-butylamine (3 g, 41 mmol) were dissolved in methanol (137 mL) under 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 8.0 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-0baa1017354342078af5de1ef510927b
Source noteuspto-grants-1998_07