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HRID 127718Erstellt: 25. Oktober 2026

Hydrochloric Acid → 3-Isoxazolamine, 5-(1,1-dimethylethyl)-

https://huagongshe.com/reaction/127718

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
EduktPentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
EduktHydroxylamine, sulfate (1:1)HCID 159255—
KatalysatorSodium HydroxideHCID 14798—
LösungsmittelWaterHCID 962—
Produkt3-Isoxazolamine, 5-(1,1-dimethylethyl)-HCID 171473123,3%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of pivaloylacetonitrile (25.03 g) and 48% sodium hydroxide (18.16 g) in water (319 ml) is added a solution of hydroxylamine sulfate (18.06 g) in water (72 ml) and the mixture is adjusted to pH 8.10±0.05 with 5% sodium hydroxide (0.38 g), stirred at 60° C. for 18 hours, mixed with 36% hydrochloric acid (26.13 g) and stirred at 70° C. for 30 minutes. Then, 36% hydrochloric acid (40.31 g) is added to the reaction mixture, which is refluxed for 40 minutes under stirring. The mixture is evaporated under atmospheric pressure to recover pinacolone (1.07 g; yield, 5.3%) and cooled to ordinary temperature. After cooling, the reaction mixture is adjusted to pH 11.8 with 48% sodium hydroxide (58.08 g) and shaken with chloroform. The chloroform layer is washed with water and concentrated under reduced pressure to give 3-amino-5-t-butylisoxazole (23.80 g). Purity, 96.6%. Yield, 84.9%. No by-product, 3-(3-t-butyl-5-isoxazolyl)amino-5-t-butylisoxazole, is detected.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04256899
Quelldatensatzuspto-grants-1981_03
ORD IDord-1ee6033f60f54e87a0f26d0d227abee1
Quellennotizuspto-grants-1981_03