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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781172Generated: October 31, 2026

4-Phenoxybenzaldehyde → HCID 19069360, compound

https://huagongshe.com/reaction/1781172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxybenzaldehydeHCID 66139—
ReactantCyclopropanemethanamineHCID 75646—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductHCID 19069360HCID 1906936078.4%

Reaction Steps

4-Phenoxybenzaldehyde (3.0 g, 15.1 mmol) and cyclopropylmethylamine (1.1 g, 15.1 mmol) were dissolved in methanol (85 mL) under a nitrogen at room temperature. Sodium cyanoborohydride (0.95 g, 15.1 mmol) was added, and stirring was continued for 48 hours. The solvent was evaporated, 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 3.0 g (78%) of the title compound as a colorless oil. 1H NMR (CDCl3, 300 MHz) δ 0.08-0.15 (m, 2H), 0.45-0.55 (m, 2H), 0.93-1.05 (m, 1H), 1.45 (br s, 1H), 2.50 (d, J=7.5 Hz, 2H), 3.78 (s, 2H), 6.95-7.03 (m, 4H) 7.05-7.13 (m, 1H), 7.25-7.38 (m, 4H). MS (DCl/NH3) m/e 254 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631401
Source datasetuspto-grants-1997_05
ORD IDord-f2de4ea21ddf47a4ae1d1a025ccb0681
Source noteuspto-grants-1997_05