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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181336Generated: November 3, 2026

4-(Benzyloxy)benzoic acid → 4-(Benzyloxy)-N-methoxy-N-methylbenzamide

https://huagongshe.com/reaction/1181336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Benzyloxy)benzoic acidHCID 73880—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product4-(Benzyloxy)-N-methoxy-N-methylbenzamideHCID 1131177794.2%

Reaction Steps

4-Benzyloxybenzoic acid (5.0 g) and N,O-dimethyl-hydroxylamine hydrochloride (2.5 g) were suspended in dimethylformamide (50 ml), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (5.0 g), 1-hydroxybenzotriazole (3.5 g) and triethylamine (3.6 ml) were added. The mixture was stirred overnight at room temperature. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water, saturated aqueous sodium hydrogencarbonate, water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (5.6 g, yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285551B2
Source datasetuspto-grants-2007_10
ORD IDord-917e877a06dc441db77d78adc156e15f
Source noteuspto-grants-2007_10