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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402537Generated: October 26, 2026

Benzyl Alcohol → 5-benzyloxy-N-methyl-2-nitroaniline

https://huagongshe.com/reaction/2402537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant5-fluoro-N-methyl-2-nitroanilineHCID 22905774—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
Product5-benzyloxy-N-methyl-2-nitroanilineHCID 6795405192%

Reaction Conditions

Temperature65 °C

Reaction Steps

Benzyl alcohol (49.6 mL, 0.48 mol), tetrabutyl ammonium chloride (6.66 g, 24.0 mmol) and potassium carbonate (40.0 g, 0.29 mol) were added to a toluene solution (200 mL) of 5-fluoro-N-methyl-2-nitroaniline (40.8 g, 0.24 mol), and the mixture was heated under reflux for 3.5 hours. The reaction solution was cooled, and 100 mL of water was added thereto. Thereafter, the mixture was stirred for 1 hour at 60 to 70° C. After the mixture was stirred under ice cooling for 30 minutes, precipitated crystals were collected by filtration. The resulting crystals were washed with water, and dried at 50° C., thereby obtaining 57.1 g of an orange, powdery target compound (yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796447B2
Source datasetuspto-grants-2014_08
ORD IDord-84d11c1ff692429b937d7e4794629a99
Source noteuspto-grants-2014_08