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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1506438Erstellt: 25. Oktober 2026

Hydroxyamine hydrochloride → (NE)-N-[[4-bromo-2-[3-[5-phenyl-4-(trifluoromethyl)-1,2-oxazol-3-yl]prop-2-ynoxy]phenyl]methylidene]hydroxylamine

https://huagongshe.com/reaction/1506438

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroxyamine hydrochlorideHCID 443297—
EduktSodium AcetateHCID 517045—
Edukt4-Bromo-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)prop-2-ynyloxy)benzaldehydeHCID 86669907—
LösungsmittelMethanolHCID 887—
Produkt(NE)-N-[[4-bromo-2-[3-[5-phenyl-4-(trifluoromethyl)-1,2-oxazol-3-yl]prop-2-ynoxy]phenyl]methylidene]hydroxylamineHCID 8729407097%

Reaktionsschritte

A mixture of 4-bromo-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)prop-2-ynyloxy)benzaldehyde (Preparation 62D, 0.050 g, 0.111 mmol), hydroxylamine hydrochloride (9.26 mg, 0.133 mmol), and sodium acetate (0.018 g, 0.222 mmol) in methanol (2.0 mL) was heated at reflux for 30 min. The solvent was removed under reduce pressure, and the residue was diluted with dichloromethane, washed with water, and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded (E)-4-bromo-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)prop-2-ynyloxy)benzaldehyde oxime (0.050 g, 0.107 mmol, 97% yield) as a white solid. The product had an HPLC with a ret. time=3.26 min.−Column: Chromolith SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA. LC/MS M+1=466.8.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09216972B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-94b3a796633f4bb38f1b5aa9560f9d56
Quellennotizuspto-grants-2015_12