Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperonyl alcohol | HCID 10322 | — |
| Reactant | 8-Methylnonanoic acid | HCID 111470 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 24890394 | HCID 24890394 | 84.4% |
Reaction Steps
Piperonyl alcohol (442 mg, 2.90 mmol), 8-methylnonanoic acid (500 mg, 2.90 mmol) and Novozyme 435 (50 mg) were measured and placed in a flask (25 ml). The mixture was stirred with heating in an oil bath at 50° C. for 16 hr without plugging the flask. After stirring with heating for 2 to 3 hr, attachment of water onto the upper wall of the flask was observed. The reaction mixture was allowed to cool to room temperature, hexane (25 ml) was added, and Novozyme 435 and the precipitated piperonyl alcohol were removed by filtration. Hexane (25 ml) was added to the filtrate, and the mixture was washed with 5% aqueous citric acid solution (25 ml×2) and saturated brine (25 ml) and dried over anhydrous magnesium sulfate. Magnesium sulfate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was developed by PTLC (preparative thin layer chromatography, Merch Art. 13895) (n-hexane:ethyl acetate=4:1), and silica gel containing the object product was stirred with ethyl acetate (100 ml) for 30 min for extraction. The silica gel was filtered off, and the filtrate was concentrated under reduced pressure to give piperonyl 8-methylnonanoate (0.75 g, yield 84.3%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981460B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-ac360659d10e487cbc1699693e20184b |
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| Source note | uspto-grants-2011_07 |
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