Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255992Generated: October 30, 2026

Hydrofluoric Acid → 1-Fluoro-5-methoxy-2-methyl-4-nitrobenzene

https://huagongshe.com/reaction/1255992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrofluoric AcidHCID 14917—
Reactant5-Methoxy-2-methyl-4-nitroanilineHCID 602726—
ReactantAcetone cardiceHCID 18522661—
ReactantSodium NitriteHCID 23668193—
SolventPyridineHCID 1049—
Product1-Fluoro-5-methoxy-2-methyl-4-nitrobenzeneHCID 1846814163%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Hydrogen fluoride (70%) in pyridine (47.4 ml, 0.48 mol) in a plastic separatory funnel was added dropwise over 20 min. to pyridine (16 mL) in a plastic bottle at −78° C. (dry ice/acetone bath) under nitrogen. Note: reaction was exothermic. After the addition was complete, the reaction was stirred for 10 min. at −78° C. 5-Methoxy-2-methyl-4-nitroaniline (9.11 g, 0.05 mol) was then added and the reaction mixture was stirred for an additional 10 min. at −78° C. Sodium nitrite (5.8 g, 0.08 mol) was then added and the reaction mixture was stirred an additional 10 min. at −78° C. The reaction mixture was allowed to warm to RT and then heated to 60° C. for 2 h. The reaction mixture was then allowed to cool to RT and an ice/water mixture (300 mL) was added. The resultant precipitates were collected by vacuum filtration, washed with water and dried under vacuum. The solid product was recrystallized from methylcyclohexane to give yellow crystals as the title product (5.8 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461170B2
Source datasetuspto-grants-2013_06
ORD IDord-dbb57ca349764c0e92bc5ee9363558bd
Source noteuspto-grants-2013_06