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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480032Generated: October 30, 2026

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

https://huagongshe.com/reaction/480032

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 numberUS06649620B2
Source datasetuspto-grants-2003_11
ORD IDord-cacdcd702acd45d49095cd387f4aef61
Source noteuspto-grants-2003_11