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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250735Generated: November 2, 2026

2-Fluoro-5-nitrobenzonitrile → 5-Amino-2-fluorobenzonitrile

https://huagongshe.com/reaction/1250735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-nitrobenzonitrileHCID 519417—
SolventEthyl AcetateHCID 8857—
Product5-Amino-2-fluorobenzonitrileHCID 273767385.4%

Reaction Steps

To a solution of 2-fluoro-5-nitrobenzonitrile (2.0 g) in ethylacetate (50 mL) was added stannous chloride dihydrate (27.0 g). The mixture was brought to reflux for 1.5 h and allowed to cool. The mixture was partitioned between ethyl acetate and sodium bicarbonate (sat. in water). The aqueous phase was extracted with ethyl acetate four times. The organic phase was washed with 4×H2O, dried over sodium sulfate, filtered and concentrated to leave 4-fluoro-3-cyanoaniline (1.40 g). CI mass spectrum z (rel. intensity) 137 (M+H, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339099B1
Source datasetuspto-grants-2002_01
ORD IDord-a31d6af66eb34dde92cf5fb20c0bda23
Source noteuspto-grants-2002_01