Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096980Generated: October 30, 2026

Acetohydroxamic Acid → HCID 59383899, compound

https://huagongshe.com/reaction/2096980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydroxamic AcidHCID 1990—
ReactantDimethylformamideHCID 6228—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-Fluoro-3-iodo-4-methylbenzonitrileHCID 59383898—
ProductHCID 59383899HCID 5938389981%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450341B2
Source datasetuspto-grants-2013_05
ORD IDord-8111a3c02c2848f4a0b1543822d6a961
Source noteuspto-grants-2013_05