Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nonan-5-ol | HCID 12202 | — |
| Reactant | 2-Iodo-5-methylbenzoic acid | HCID 142941 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | 5-Nonanone | HCID 10405 | — |
Reaction Steps
1.57 mg (0.006 mmol) of 2-iodo-5-methylbenzoic acid prepared by Preparation Example 3, 1.11 g (1.8 mmol) of powdered Oxone (registered trademark) and 433 mg (3 mmol) of 5-nonanol were added to 3.75 ml of nitromethane, and the mixture was heated at 70° C. while being stirred for 12 hours. After being heated, the mixture was cooled to room temperature, and the insoluble substance was removed by means of filtering. Water was added in the filtrate, extraction was carried out using diethyl ether. The organic phase was dried by using sodium sulfate, and then 5-nonanone was obtained by means of vacuum-concentration. The yield of the obtained 5-nonanone was determined and the result is shown in Table 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-28d804917361414e816455430fceb2de |
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| Source note | uspto-grants-2013_03 |
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