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 | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Nonanone | HCID 10405 | — |
Reaction Steps
7.86 mg (0.03 mmol) of 2-iodo-5-methylbenzoic acid prepared by Preparation Example 3, 1.48 g (2.4 mmol) of Oxone (registered trademark) and 433 mg (3 mmol) of 5-nonanol were added to 3.75 ml of ethyl acetate, 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 to 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 the 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-15179f767bbc4659b836ea6d59208db9 |
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| Source note | uspto-grants-2013_03 |
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