Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Geraniol | HCID 637566 | — |
| Reactant | Sodium 2-Iodobenzenesulfonate | HCID 23662047 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | Citral | HCID 638011 | — |
Reaction Steps
6.1 mg (0.02 mmol) of sodium 2-iodobenzenesulfonate prepared by Preparation Example 4, 0.37 g (0.6 mmol) of powdered Oxone (registered trademark), 0.5 g (3.5 mmol) of anhydrous sodium sulfate and 154 mg (1 mmol) of (E)-3,7-dimethylocta-2,6-dien-1-ol were added to 5 ml of nitromethane, and the mixture was heated at 70° C. while being stirred under a nitrogen for two hours. The later treatment was carried out in the same way as in Example 1, and then (E)-3,7-dimethylocta-2,6-dienal was obtained. The yield of the obtained (E)-3,7-dimethylocta-2,6-dienal was determined and the result is shown in Table 2. (Yield: E:Z=16:1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394995B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-f1d3de82320a4deaa4f18892dad51481 |
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| Source note | uspto-grants-2013_03 |
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