Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-acetyl-4-methyl-4-pentenoate | HCID 536075 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | HCID 73447335 | HCID 73447335 | — |
Reaction Steps
At 10° C., 200 g of methyl 2-acetyl-4-methylpent-4-enoate (preparation: cf. Tetrahedron (1985) 4633) in 2000 ml of aqueous 10% strength potassium hydroxide solution were admixed with 85 g of sodium nitrite, and the mixture was stirred at 23° C. for 18 hours. With ice-cooling, 1000 ml of 10% strength sulfuric acid were subsequently added dropwise such that the internal temperature remained below 10° C. The mixture was then stirred at 10° C. until evolution of CO2 had ceased. For work-up, the mixture was extracted with methyl tert-butyl ether, the combined organic phases were extracted with 3 N aqueous sodium hydroxide solution and the alkaline phases were adjusted to pH 1 using 20% strength sulfuric acid. They were then extracted with methylene chloride, the extract was dried over sodium sulfate and the solvent was removed under reduced pressure. This gave 142 g of the title compound as a yellow oil which crystallized on standing.
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-7b550e9296ce40d881e5912f97a8bdc6 |
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| Source note | uspto-grants-2002_02 |
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