Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nonan-5-ol | HCID 12202 | — |
| Reactant | 2-iodobenzenesulfonic Acid | HCID 2778247 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Nonanone | HCID 10405 | — |
Reaction Steps
8.5 mg (0.03 mmol) of 2-iodobenzenesulfonic acid prepared by Preparation Example 1, 1.48 g (2.4 mmol) of Oxone (registered trademark) and 433 mg (3 mmol) of 5-nonanol were added to 3.75 ml ethyl acetate, and the mixture was heated at 70° C. while being stirred for ten hours. After heating, the mixture was cooled to room temperature, and the insoluble substance was removed by means of filtering. The obtained filtrate was vacuum-concentrated, and diethyl ether is added in the residue, and then an insoluble material was removed by filtering. The obtained filtrate was vacuum-concentrated, and then 5-nonanone was obtained. 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-28c73ddca10b456cb3298d9e9bc6ada1 |
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| Source note | uspto-grants-2013_03 |
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