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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010409Generated: October 25, 2026

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

https://huagongshe.com/reaction/1010409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantTetrahydrofuran ethyl acetateHCID 21939870—
ReactantN-{1-(1H-Benzotriazolyl)methyl}-4-benzyloxy-2-fluoroanilineHCID 22936313—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductN-Methyl-4-benzyloxy-2-fluoroanilineHCID 2293665864.9%

Reaction Steps

After dissolving N-{1-(1H-benzotriazolyl)methyl}-4-benzyloxy-2-fluoroaniline (14.13 g, 40.56 mmol) in N,N-dimethylformamide (200 ml), methanol (150 ml) and ethanol (50 ml), there was added sodium borohydride (3.06 g, 81.12 mmol) and the mixture was stirred for 2.5 hours at room temperature. There was further added sodium borohydride (0.78 g, 20.28 mmol), and the mixture was stirred for 13.5 hours at room temperature. Water was added to the reaction solution, extraction was performed with ethyl acetate-tetrahydrofuran, 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 system) to obtain the title compound (5.98 g, 26.31 mmol, 64.87%) as light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-297515d9fc1b4a9d9d7c0295af7fbe67
Source noteuspto-grants-2011_07