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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516548Generated: October 25, 2026

Hydroxyamine hydrochloride → (NE)-N-[(4-bromo-2,5-difluorophenyl)methylidene]hydroxylamine

https://huagongshe.com/reaction/516548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant4-Bromo-2,5-difluorobenzaldehydeHCID 22489081—
SolventEthanolHCID 702—
SolventPyridineHCID 1049—
SolventAmmonium ChlorideHCID 25517—
Product(NE)-N-[(4-bromo-2,5-difluorophenyl)methylidene]hydroxylamineHCID 9031047153.5%

Reaction Steps

A solution of 4-bromo-2,5-difluorobenzaldehyde (7.0 g, 31.67 mmol), hydroxyl amine hydrochloride (2.42 g, 34.84 mmol) in pyridine (35 mL) and ethanol (35 mL) was stirred at room temperature for 30 min. The reaction mixture was diluted with saturated ammonium chloride solution and extracted with ethyl acetate. The organic phase was washed with saturated brine solution, dried (Na2SO4), filtered, and concentrated under reduced pressure. The crude product was purified by flash chromatography (SiO2, eluting with 5-100% ethyl acetate in hexanes) to provide the title compound as a yellow solid (4.0 g, 53%): ESIMS m/z 238 [(M+2H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09113629B2
Source datasetuspto-grants-2015_08
ORD IDord-2b742c3ec23b4560b2f4e16afbf75d16
Source noteuspto-grants-2015_08