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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128434Generated: October 30, 2026

Water → 3-Isoxazolamine, 5-(1,1-dimethylethyl)-

https://huagongshe.com/reaction/128434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantPentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventEthanolHCID 702—
Product3-Isoxazolamine, 5-(1,1-dimethylethyl)-HCID 17147373.6%

Reaction Steps

In a 100 ml. round bottom flask there was placed 2 g. of pivalyl acetonitrile, 0.64 g. of sodium hydroxide, 35 ml. of water, and 25 ml. of ethanol. This mixture was heated to reflux and the pH was determined to be about 8.9. Then an aqueous solution of 1.0 g. of hydroxylamine hydrochloride was slowly added. At the end of the addition the pH was about 6.3. The pH of the reaction mixture was adjusted to about 6.5. After 1 hour, the pH was about 6.3 and was again adjusted to about 6.5. After 2 hours the pH was observed to be about 7.0 and was again adjusted to pH about 6.5. At 3 hours and again at 4 hours, the pH was determined to be about 6.5. The reaction mixture was allowed to reflux overnight and the following morning the pH was determined to be about 6.1. The ethanol was removed using a rotovapor and a yellow solid precipitated. This solid was filtered off and dried. It weighed 1.1 g. and it was determined by vpc to contain 94.2% of 3-amino-5-(t-butyl)isoxazole and 3.7% of 5-amino-3-(t-butyl)isoxazole. The product had a melting point of about 103°-105° C. Yield: 73.6% of desired isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259501
Source datasetuspto-grants-1981_03
ORD IDord-2c6f58409e834337b6f44422c58d31ed
Source noteuspto-grants-1981_03