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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660260Generated: October 29, 2026

Ethanol → 3-Fluoro-N-hydroxy-4-methylbenzamidine

https://huagongshe.com/reaction/660260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydroxylamineHCID 787—
Reactant3-Fluoro-4-methylbenzonitrileHCID 585140—
SolventWaterHCID 962—
Product3-Fluoro-N-hydroxy-4-methylbenzamidineHCID 273737591.6%

Reaction Steps

To a suitable vessel equipped with mechanical stirrer under N2 atmosphere was charged 202.0 g of 3-fluoro-4-methylbenzonitrile followed by 1.0 L of ethanol. Hydroxylamine (144 mL of 50% solution in water) was added via addition funnel over 20 minutes. The mixture was stirred at ambient temperature until HPLC analysis showed that reaction was complete (no starting material remained). Water (3.0 L) was added dropwise to the pale yellow solution over 1 hour to give a thick slurry. The slurry was cooled in an ice water bath to 2° C. for 1.5 hours, filtered and dried under vacuum at 35° C. for 22 hours to give the title compound (230.3 g, 91.6%) as a white solid. 1H-NMR (CDCl3, 500 MHz) 67.30 (m, 2H), 7.19 (m, 1H), 4.87 (s, 2H), 2.28 (s, 3H); 13C-NMR (CDCl3, 500 MHz) δ162.15, 160.19, 151.58, 131.82, 131.76, 131.66, 131.62, 127.01, 126.87, 121.06, 112.69, 112.51, 14.48; 19F-NMR (CDCl3, 500 MHz) δ−116.35, −116.37, −116.39. LC-MS M+H169.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084477B2
Source datasetuspto-grants-2011_12
ORD IDord-cb25657a3e2c43dbb9b26986a88b30f9
Source noteuspto-grants-2011_12