HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096980Generated: October 30, 2026
Acetohydroxamic Acid → HCID 59383899, compound
https://huagongshe.com/reaction/2096980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetohydroxamic Acid | HCID 1990 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2-Fluoro-3-iodo-4-methylbenzonitrile | HCID 59383898 | — |
| Product | HCID 59383899 | HCID 59383899 | 81% |
Reaction Steps
Potassium tert-butoxide (2.20 g, 19.2 mmol) was added to a solution of N-hydroxyacetamide (1.44 g, 19.2 mmol) in N,N′-dimethylformamide (25 mL) under argon. The resulting white suspension was stirred at room temperature for 30 minutes and then 2-fluoro-3-iodo-4-methylbenzonitrile (WO2006094187, 2.00 g, 7.7 mmol) was added and the mixture was stirred at room temperature for 6 hours. Further N-hydroxyacetamide (0.29 g, 3.9 mmol) and potassium tert-butoxide (0.45 g, 3.9 mmol) were added and the mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure and water and ethyl acetate were added. The organic layer was separated and the aqueous phase was extracted with further ethyl acetate. The combined organic layers were washed with brine, dried, (MgSO4) and evaporated. The residue was purified by flash chromatography (9:1 hexanes/ethyl acetate to ethyl acetate) to yield the title compound (1.79 g, 81%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450341B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-8111a3c02c2848f4a0b1543822d6a961 |
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| Source note | uspto-grants-2013_05 |
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