HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128435Generated: October 30, 2026
Water → 3-Isoxazolamine, 5-(1,1-dimethylethyl)-
https://huagongshe.com/reaction/128435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Pentanenitrile, 4,4-dimethyl-3-oxo- | HCID 108871 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Isoxazolamine, 5-(1,1-dimethylethyl)- | HCID 171473 | 72.9% |
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. The pH of the mixture was determined to be about 8.6. Then 1.1 g. of hydroxylamine hydrochloride in 15 ml. of water was added dropwise. At the end of the addition the pH of the reaction mixture was about 5.1. The pH of the reaction mixture was adjusted to about 7.0. After 1 hour the pH was determined to be about 7.6 and was adjusted back to about 7.0. After 2 hours the pH was determined to be about 6.9 and was readjusted to about 7.0. After 3 hours the pH was determined to be about 7.5 and was adjusted to about 7.0. After 4 hours the pH was determined to be about 6.8 and was readjusted to about 7.0. The reaction mixture was allowed to reflux overnight and the following morning the pH was determined to be about 6.3 and was readjusted to about 7.0. The ethanol solvent was stripped using a rotovapor and a yellow solid precipitated. The solid was filtered off and dried. The solid weighed 1.1 g. and had a melting point of about 101°-104° C. It was determined by vpc to contain 92.6% of 3-amino-5-(t-butyl)isoxazole and 4% of 5-amino-3-(t-butyl)isoxazole. Yield: 72.9% of desired isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04259501 |
|---|
| Source dataset | uspto-grants-1981_03 |
|---|
| ORD ID | ord-9c493092b0e54308b35daff60b284786 |
|---|
| Source note | uspto-grants-1981_03 |
|---|