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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127714Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/127714

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
EduktPentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
EduktHydroxylamine, sulfate (1:1)HCID 159255—
KatalysatorSulfuric AcidHCID 1118—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
Produkt3-Isoxazolamine, 5-(1,1-dimethylethyl)-HCID 171473125,1%

Reaktionsschritte

To a suspension of pivaloylacetonitrile (25.03 g) in water (400 ml) is added 96% sodium hydroxide (9.17 g). Hydroxylamine sulfate (18.06 g) is added to the resulting solution at 27° C. The mixture is stirred at room temperature for 30 minutes, adjusted to pH 8 with 10% sulfuric acid (0.97 g), stirred at 60° C. for 22 hours, cooled at 20° C., mixed with conc. hydrochloric acid (7.90 g), and heated at 50° C. for 2 hours. Conc. hydrochloric acid (14.18 g) is added to the mixture, which is heated at 100° C. for 1 hour. After cooling, the reaction mixture is adjusted to pH 11 with 30% sodium hydroxide (49.8 g) and shaken with chloroform. The organic layer is washed with water, dried over anhydrous sodium sulfate and concentrated to remove chloroform, whereby 3-amino-5-t-butylisoxazole (24.16 g) is obtained. Yield, 86.2%. Purity, 95.4%. m.p. 103.5-109° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04256899
Quelldatensatzuspto-grants-1981_03
ORD IDord-b4908edb535c4a73bfe5fb627436f4d4
Quellennotizuspto-grants-1981_03