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HRID 452573Erstellt: 24. Oktober 2026

Hydroxyamine hydrochloride → N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimine

https://huagongshe.com/de/reaction/452573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroxyamine hydrochlorideHCID 443297—
Edukt(1-methyl-1H-tetrazol-5-yl)[3-(trifluoromethoxy)phenyl]methanoneHCID 67075092—
LösungsmittelPyridineHCID 1049—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimineHCID 13633738592%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a stirred solution of (1-methyl-1H-tetrazol-5-yl)[3-(trifluoromethoxy)phenyl]methanone (5.12 g, 16.2 mmol) in dry pyridine (25 mL) was added hydroxylamine hydrochloride (2.81 g, 40.4 mmol). The mixture was stirred at 70° C. for 3 h, then left to stand overnight. After concentration of the reaction mixture in vacuo, the residue was diluted with ethyl acetate (100 mL) and washed with water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL), the combined organic layers dried (MgSO4), concentrated in vacuo and dissolved in toluene. A crystalline precipitate appeared, which was filtered off to afford N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimine as a white solid [4.33 g, yield 92%; HPLC/MS:m/z=288 (M+H); log P(HCOOH)=2.37].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08492388B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-9a719dbbe32c4adcb817e72b8d34ec10
Quellennotizuspto-grants-2013_07