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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010404Generated: October 27, 2026

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

https://huagongshe.com/reaction/1010404

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 brine 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 numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-91f8bdb10a654ebebb34ac3d7bd5ee70
Source noteuspto-grants-2011_07