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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113455Generated: October 29, 2026

Hydroxyamine hydrochloride → HCID 86246798, compound

https://huagongshe.com/reaction/2113455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
Reactant2-Chloro-3,6-difluorobenzaldehydeHCID 2773509—
SolventEthanolHCID 702—
ProductHCID 86246798HCID 86246798—

Reaction Steps

A solution of 2-chloro-3,6-difluoro-benzaldehyde (16.5 g, 93 mmol) in ethanol (80 ml) was treated with hydroxylamine HCl (7.80 g, 112 mmol) and sodium acetate (9.20 g, 112 mmol). The mixture was heated under reflux for 16 h, then the solvent was evaporated, and the residue stirred with water. The precipitate was filtered and dried to afford 2-chloro-3,6-difluoro-benzaldehyde oxime. It was dissolved in acetic anhydride (140 ml) and refluxed for 16 h, then the mixture was evaporated to afford 2-chloro-3,6-difluoro-benzonitrile as a light brown liquid (10.6 g, 65%). In analogy to example 5a, this compound was reacted with 4-methylimidazole and potassium carbonate for 20 h at 90° C. Aqueous workup, extraction with Ethyl acetate followed by chromatography (SiO2, dichloromethane:methanol=100:0 to 97:3) afforded the title compound as a white solid (yield: 6%). MS: m/e=336.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432256B2
Source datasetuspto-grants-2008_10
ORD IDord-f2b827448ab24763ac42d186770d8246
Source noteuspto-grants-2008_10