Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 73447335 | HCID 73447335 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 54272823 | HCID 54272823 | — |
Reaction Steps
285.7 g of 5-methylhex-5-ene-2,3-dione 3-oxime from Example 1 were dissolved in 750 ml of acetone and admixed with 335.8 g of potassium carbonate. 362 g of diethyl sulfate in 300 ml of acetone were then added dropwise, and the mixture was stirred at 23° C. for 2 hours. The solvent was subsequently removed under reduced pressure, the residue was taken up in methyl tert-butyl ether/water and the aqueous phase was extracted again with methyl tert-butyl ether. The combined organic phases were washed with 15% strength ammonia solution and water and dried over sodium sulfate, and the solvent was removed under reduced pressure. This gave 355.4 g of the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06344589B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-75504b453c874d2da164bea9a48c1731 |
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| Source note | uspto-grants-2002_02 |
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