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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275935Generated: October 29, 2026

Acetic Acid → 4-Fluoro-3-nitrophenol

https://huagongshe.com/reaction/1275935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric AcidHCID 1118—
ReactantPeracetic AcidHCID 6585—
Reactant4'-Fluoro-3'-nitroacetophenoneHCID 2734612—
SolventWaterHCID 962—
Product4-Fluoro-3-nitrophenolHCID 1675186120%

Reaction Steps

Concentrated sulfuric acid (200 mL) and acetic acid (120) mL are mixed at 0° C. To this solution is added 15 g (0.082 mol) of 4-fluoro-3-nitroacetophenone with stirring. To the cold reaction mixture is added 36 mL of 36% peracetic acid. The reaction mixture is then stirred at room temperature for 4 hours. Water (500 mL) is added to the mixture, and the crude product is extracted into diethyl ether. The combined ether fractions are washed with water, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified using column chromatography on silica gel, eluting with 3% methanol/chloroform, giving 3.2 g of Compound 23 (20% yield). mp: 86-87° C. 1H-NMR (CDCl3) 7.56 (dd, 1H); 7.29 (t, 1H), 7.12 (m, 1H); 5.36 (s, 1H). 19F-NMR (d6 -DMSO) 147.60 (s). Anal. calc. for C6H4FNO3 : C, 45.87; H, 2.57; N, 8.92. Found: C, 45.80; H. 2.51; N, 8.69.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162931
Source datasetuspto-grants-2000_12
ORD IDord-f208fbe6b6054b8dacf86edd1bd8a18b
Source noteuspto-grants-2000_12