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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244332Generated: October 26, 2026

Water → 1-Chloro-2-fluoro-4-(2-nitro-vinyl)-benzene

https://huagongshe.com/reaction/2244332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantNitromethaneHCID 6375—
ReactantAmmonium AcetateHCID 517165—
Reactant4-Chloro-3-FluorobenzaldehydeHCID 2724985—
SolventAcetic AcidHCID 176—
Product1-Chloro-2-fluoro-4-(2-nitro-vinyl)-benzeneHCID 6680171266%

Reaction Steps

4-Chloro-3-fluorobenzaldehyde (13 g, 82 mmol) and ammonium acetate (14.6 g, 189 mmol) were dissolved in acetic acid (150 ml) and nitromethane (12.6 ml, 234 mmol) was added. The solution was heated to reflux for 1.5 h. After cooling to RT water (120 ml) was added. A solid precipitated. The reaction was extracted three times with methylene chloride. The combined organic layers were washed with water and sat. aq. NaCl solution, dried over magnesium sulfate, filtered and the solvent was removed in vacuo. The residue was purified by flash column chromatography (Ethyl acetate/cyclohexane:1/4). The crude product was suspended in heptane, filtered and dried to yield 1-chloro-2-fluoro-4-(2-nitro-vinyl)-benzene (10.9 g, 66%) as a light yellow solid. 1H NMR (CDCl3, 300 MHz): δ 7.29 (d, J=7.8 Hz, 1H), 7.33 (d, J=9.3 Hz, 1H), 7.50 (t, J=7.5H, 1H), 7.54 (d, J=13.6 Hz, 1H), 7.92 (d, J=13.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678818B2
Source datasetuspto-grants-2010_03
ORD IDord-673eaf4aff154051aa3cf586759c92df
Source noteuspto-grants-2010_03