HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793676Generated: November 2, 2026
Hydrochloric Acid → 3-Fluoro-4-iodobenzaldoxime
https://huagongshe.com/reaction/1793676
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrone | HCID 6350 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Fluoro-4-iodoaniline | HCID 15475546 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Fluoro-4-iodobenzaldoxime | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07081538B1 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-a62c224cbe324dcb99aa2eed4a2acf87 |
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| Source note | uspto-grants-2006_07 |
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