HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544381Generated: October 30, 2026
Hydroxyamine hydrochloride → 2-Oxo-4,5,5-trimethyl-3-thiazoline oxime
https://huagongshe.com/reaction/544381
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methyl-3-oxobutan-2-yl thiocyanate | HCID 14195165 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Oxo-4,5,5-trimethyl-3-thiazoline oxime | HCID 85997244 | — |
Reaction Steps
8.3 g (0.12 mol) of hydroxylamine hydrochloride are dissolved in 50 ml of water and treated with 10.1 g (0.12 mol) of sodium bicarbonate. This solution (pH 6-7) is added at room temperature while stirring to a solution of 14.3 g (0.1 mol) of 3-methyl-3-thiocyanato-2-butanone in 100 ml of ethanol. The temperature of the mixture rises rapidly to 37° C. The mixture is subsequently stirred for an additional 1 hour and 120 mlof the solvent are distilled off at 50° C. under reduced pressure. The residue is extracted three times with 100 ml of diethyl ether each time and the organic phase is washed with a small amount of water, dried over anhydrous sodium sulfate and concentrated until crystallization begins. After cooling, the crystal slurry is treated with 10 ml of n-hexane. The crystals are filtered off under suction, washed with diethylether/n-hexane (2:1) and dried to yield 2-oxo-4,5,5-trimethyl-3-thiazoline oxime, m.p. 151°-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04450157 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-c903caf11cc644d48d001cbcc7ca7f2b |
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| Source note | uspto-grants-1984_05 |
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