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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430418Generated: November 2, 2026

Benzyl Alcohol → 3-benzyloxy-2-nitro-N-methylaniline

https://huagongshe.com/reaction/1430418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant3-fluoro-N-methyl-2-nitroanilineHCID 54489739—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product3-benzyloxy-2-nitro-N-methylanilineHCID 10729890100%

Reaction Steps

Benzyl alcohol (9.54 mL, 92.2 mmol), tetrabutyl ammonium bromide (1.49 g, 4.62 mmol), and potassium carbonate (7.64 g, 55.3 mmol) were added to a toluene solution (39 mL) of 3-fluoro-N-methyl-2-nitroaniline (7.84 g, 46.1 mmol), and the mixture was heated under reflux for 6 hours. The reaction solution was cooled, and water (39 mL) was added thereto, followed by toluene extraction. The resulting organic layer was washed with water, and the solvent was distilled off under reduced pressure, thereby obtaining 11.9 g of a red, powdery target compound (yield: 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940889B2
Source datasetuspto-grants-2015_01
ORD IDord-36111e3a7df94f0c88679ea55cd1d94a
Source noteuspto-grants-2015_01