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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510989Generated: October 27, 2026

Water → Homovanillyl 8-methylnonanoate

https://huagongshe.com/reaction/1510989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHomovanillyl alcoholHCID 16928—
Reactant8-Methylnonanoic acidHCID 111470—
SolventEthyl AcetateHCID 8857—
ProductHomovanillyl 8-methylnonanoateHCID 2482302893.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

Homovanillyl alcohol (769 mg, 4.57 mmol), 8-methylnonanoic acid (751 mg, 4.35 mmol) and Novozyme 435 (51 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, ethyl acetate (25 ml) was added, and Novozyme 435 and the precipitated insoluble material were removed by filtration. Ethyl acetate (50 ml) was added to the filtrate, and the mixture was washed with 5% aqueous citric acid solution (25 ml×2), saturated brine (25 ml), 5% aqueous sodium hydrogen carbonate 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) (n-hexane:ethyl acetate=3:1), 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 homovanillyl 8-methylnonanoate (1.31 g, yield 93.2%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212068B2
Source datasetuspto-grants-2012_07
ORD IDord-c63ecb5ee4264ba0be74e8c83b5747bf
Source noteuspto-grants-2012_07