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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793676Generated: November 2, 2026

Hydrochloric Acid → 3-Fluoro-4-iodobenzaldoxime

https://huagongshe.com/reaction/1793676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitroneHCID 6350—
ReactantSodium SulfiteHCID 24437—
ReactantSodium AcetateHCID 517045—
Reactant3-Fluoro-4-iodoanilineHCID 15475546—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product3-Fluoro-4-iodobenzaldoximeHCID 86616683—

Reaction Steps

3-Fluoro-4-iodoaniline (15.36 g, 0.069 M) and concentrated hydrochloric acid (18.51 g) were dissolved in a mixture of water (30 ml) and ice (30 g). The solution was treated at 0–5° with a solution of sodium nitrite (4.81 g, 0.07 M) in water (15 ml). The pH of the resulting red-brown solution was adjusted to 5–6 by the addition of sodium acetate (6.05 g, 0.044 M). To the solution of formaldoxime was added sodium acetate (45.38 g, 0.333 M), hydrated copper sulfate (1.72 g, 6.9 mM) and sodium sulfite (0.275 g, 2.18 mM), giving a deep green solution, which was cooled to 10–15°. The solution of the diazonium salt was then slowly introduced with vigorous stirring, and stirring continued for 1 hour. The mixture was extracted with diethyl ether (3×100 ml), the combined extracts washed with water (100 ml), and dried (magnesium sulfate). The residue after filtration and evaporation was chromatographed in four portions on 50 g silica Mega Bond Elut® columns, eluting with a gradient from dichloromethane to 5% methanol in dichloromethane. Relevant fractions were combined to give the desired product (3.52 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081538B1
Source datasetuspto-grants-2006_07
ORD IDord-a62c224cbe324dcb99aa2eed4a2acf87
Source noteuspto-grants-2006_07