Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 10878028 | HCID 10878028 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22163855 | HCID 22163855 | 86.8% |
Reaction Steps
In the course of 3 hours, 60 g (2 mols of sodium hydride (80% strength in paraffin oil) are added to a solution of 138 g (2 mols of 1,2,4-triazole in 1,600 ml of absolute dimethylformamide, with vigorous evolution hydrogen. The mixture is stirred for a further 30 minutes at room temperature. 388 g (2 mols of 3,3-dimethyl -4-[(methylsulphonyl)oxy]-2-butanone are then added dropwise in the course of 15 minutes. The reaction mixture is then stirred for 16 hours at 95° C. 100 ml of water are firstly added carefully to the reaction mixture, and the mixture is then poured into 4 1 of water. The mixture is extracted six times with dichloromethane. The combined organic phases are washed once with plenty of water, dried over sodium sulphate and concentrated under a high vacuum. After column chromatography (silica gel; dichloromethane/ethyl acetate=1:1), 290 g (86.8% of 3,3-dimethyl -4-(1,2,4-triazol-1-yl)-2-butanone are obtained as an oil with a content of 97% after GC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04960781 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-0b2d568d9ed5457683ac4fb060f8619c |
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| Source note | uspto-grants-1990_10 |
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