HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847651Generated: October 30, 2026
Isobutyryl chloride → N-(5-t-butyl-3-isoxazolyl)isobutyramide
https://huagongshe.com/reaction/847651
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | 3-Isoxazolamine, 5-(1,1-dimethylethyl)- | HCID 171473 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(5-t-butyl-3-isoxazolyl)isobutyramide | HCID 13020366 | 91.7% |
Reaction Steps
To a solution of 3-amino-5-t-butylisoxazole (2.80 g) in pyridine (10 ml) is dropwise added isobutyryl chloride (2.34 g) keeping the mixture below 10° C. The reaction mixture is stirred with cooling for 30 minutes and at room temperature for 1 hour and evaporated to remove the pyridine. The residue is mixed with 5% hydrochloric acid solution (40 ml) and shaken with methylene chloride. The methylene chloride layer is separated, washed with saturated aqueous sodium hydrogen carbonate and water, dried over anhydrous sodium sulfate and evaporated to remove the methylene chloride. The residue is chromatographed on a column of silica gel and recrystallized from n-hexane to give N-(5-t-butyl-3-isoxazolyl)isobutyramide (3.85 g) as colorless needles melting at 123.0° to 124.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04293328 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-b48792f085f5446ab6ee7d03729abadf |
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| Source note | uspto-grants-1981_10 |
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