Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178468373 | HCID 178468373 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Diacetyl(methoxyimino)methane | HCID 536122 | 89% |
Reaction Steps
In a 20 l vessel, 4.5 kg (32.6 mol) of potassium carbonate were suspended in 3.2 l of methyl tert-butyl ether and a liter of DMF. With stirring, the mixture was cooled to from 0 to −10° C. A solution of 4128 g (32 mol) of pentane-2,3,4-trione 3-oxime, 2 l of DMF and 4032 g (32 mol) of dimethyl sulfate was then metered in at an internal temperature of <25° C. over a period of 2 hours. The mixture was stirred at room temperature for another 3.5 hours. A further 20 l of water were then added, the upper, organic phase was removed, the aqueous phase was washed with 2 l of methyl tert-butyl ether, the combined organic phases were washed with 1 l of 5% strength hydrochloric acid and the solvent was distilled off. This gave 4214 g of the title compound in a purity of 96.6% (GC area percent), corresponding to a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06441236B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-c7a17002782a4f7aa124f709e0c628b1 |
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| Source note | uspto-grants-2002_08 |
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