HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012888Generated: October 25, 2026
Water → 3-Ethoxy-4-hydroxybenzyl 8-methylnonanoate
https://huagongshe.com/reaction/1012888
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 8-Methylnonanoic acid | HCID 111470 | — |
| Reactant | Ethyl vanillyl alcohol | HCID 597767 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Ethoxy-4-hydroxybenzyl 8-methylnonanoate | HCID 67316993 | 89.1% |
Reaction Steps
3-Ethoxy-4-hydroxybenzyl alcohol (733 mg, 4.35 mmol), 8-methylnonanoic acid (751 mg, 4.35 mmol) and Novozyme 435 (100 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 (50 ml) was added, and Novozyme 435 and the insoluble material 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 to give 3-ethoxy-4-hydroxybenzyl 8-methylnonanoate (1.25 g, yield 88.8%) 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-663edc46763747b4ab38b2ebb736dff6 |
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| Source note | uspto-grants-2011_07 |
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