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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522471Generated: October 30, 2026

Water → 5-Amino-2-fluoro-4-methylbenzonitrile

https://huagongshe.com/reaction/522471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
Reactant5-Bromo-4-fluoro-2-methylanilineHCID 2782786—
ReactantHCID 178418546HCID 178418546—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5-Amino-2-fluoro-4-methylbenzonitrileHCID 8667744968.5%

Reaction Conditions

Temperature180 °C

Reaction Steps

The starting 5-bromo-4-fluoro-2-methylaniline (1) (20 g, 98 mmol) was dissolved in anhydrous 1-methylpyrrolidinone (100 mL), and copper (I) cyanide (17.6 g, 196 mmol) was added. The reaction was heated to 180° C. for 3 hours, cooled to room temperature, and water (300 mL) and concentrated ammonium hydroxide (300 mL) added. The mixture was stirred for 30 minutes and extracted with EA (3×200 mL). The combined extracts were dried over magnesium sulfate, and the solvent was removed under reduced pressure. The oily residue was washed with hexanes (2×100 mL), and the solid dissolved in dichloromethane and loaded onto a silica gel column. Eluting with 0 to 25% EA in hexanes gradient provided 5-amino-2-fluoro-4-methylbenzonitrile (10.06 g, 67.1 mmol). LC/MS (m/z: 151 M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09333197B2
Source datasetuspto-grants-2016_05
ORD IDord-16fad01f38664e5b935cab11bf5e7d97
Source noteuspto-grants-2016_05