HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127234Generated: November 1, 2026
Water → 2-Oxo-4,5,5-trimethyl-3-thiazoline oxime
https://huagongshe.com/reaction/127234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methyl-3-oxobutan-2-yl thiocyanate | HCID 14195165 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Oxo-4,5,5-trimethyl-3-thiazoline oxime | HCID 85997244 | — |
Reaction Steps
8.3 g. (0.12 mol) of hydroxylamine hydrochloride were dissolved in 50 ml. of water and treated with 10.1 g. (0.12 mol) of sodium hydrogen carbonate. This solution (pH 6-7) was added with stirring at room temperature 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 rose rapidly to 37° C. The mixture was then stirred for 1 hour, 120 ml. of the solvent were then distilled off at 50° C. in vacuo. The residue was extracted three times with 100 ml. of ether each time. The organic phase was washed with a small amount of water, dried over sodium sulfate and concentrated until crystallization began. After cooling, the crystal sludge was treated with 10 ml. of hexane. The crystals were filtered off under suction, washed with ether/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 | US04255436 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-0ec2f2173ab640f7aa1b1aa7def0c7c3 |
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| Source note | uspto-grants-1981_03 |
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