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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478611Generated: October 30, 2026

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

https://huagongshe.com/reaction/478611

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 h. After cooling, the reaction mixture was partitioned between CH2Cl2 and H2O and the aqueous phase was further extracted with CH2Cl2. 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 numberUS06642242B2
Source datasetuspto-grants-2003_11
ORD IDord-4abfa68b966b46f0896f9811f25e1508
Source noteuspto-grants-2003_11