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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228485Generated: October 31, 2026

3-Benzyloxy-4-methoxybenzaldehyde → 3-(Benzyloxy)-4-methoxybenzonitrile

https://huagongshe.com/reaction/2228485

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzyloxy-4-methoxybenzaldehydeHCID 80671—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product3-(Benzyloxy)-4-methoxybenzonitrileHCID 275227689%

Reaction Steps

3-Benzyloxy-4-methoxybenzaldehyde (50 g, 0.21 mol) was added to a solution of sodium acetate (33.9 g, 0.41 mol) and hydroxylamine hydrochloride (28.73 g, 0.41 mol) in acetic acid (200 ml) and the resulting suspension was heated to reflux for 18 hours. After cooling, the reaction mixture was partitioned between dichloromethane and water and the aqueous phase was further extracted with dichloromethane. The combined organic layers were dried over MgSO4 and evaporated to afford the subtitle compound as a buff-coloured solid (43.9 g, 89%). Rf 0.70 (toluene:EtOAc 4:1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417194B1
Source datasetuspto-grants-2002_07
ORD IDord-ca860ad41c374bcaaffda13cde8f5766
Source noteuspto-grants-2002_07