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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388017Generated: October 25, 2026

Water → N-Methyl-4-benzyloxy-2-methylaniline

https://huagongshe.com/reaction/388017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1H-Benzotriazole-1-methanolHCID 224169—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(Benzyloxy)-2-methylanilineHCID 16773053—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-Methyl-4-benzyloxy-2-methylanilineHCID 2293649862.5%

Reaction Steps

After dissolving 4-benzyloxy-2-methylaniline (6.55 g, 30.72 mmol) in N,N-dimethylformamide (10 ml) and methanol (60 ml), 1H-benzotriazole-1-methanol (4.58 g, 30.72 mmol) was added and the mixture was stirred for 30 minutes at room temperature. N,N-Dimethylformamide (20 ml) was added for complete dissolution of the precipitated crystals, sodium borohydride (2.32 g, 61.44 mmol) was added in small portions at a time at room temperature (internal temperature increase), and the mixture was stirred for 30 minutes. Water was added to the reaction solution, extraction was performed ethyl acetate, the extract was washed with saturated saline and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was adsorbed onto silica gel and purified by silica gel column chromatography (hexane-ethyl acetate) to obtain the title compound (4.364 g, 19.20 mmol, 62.49%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-868b6d69f9df4049ab99b8686cccfd50
Source noteuspto-grants-2013_02