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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012886Generated: October 31, 2026

Water → Veratryl 8-methylnonanoate

https://huagongshe.com/reaction/1012886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantVeratryl alcoholHCID 7118—
Reactant8-Methylnonanoic acidHCID 111470—
SolventHexaneHCID 8058—
ProductVeratryl 8-methylnonanoateHCID 2489039589.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

Veratryl alcohol (734 mg, 4.53 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, 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. The residue was developed by PTLC (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 veratryl 8-methylnonanoate (1.25 g, yield 89.1%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981460B2
Source datasetuspto-grants-2011_07
ORD IDord-514f8b4812074714ae76fa0c4abb3dcf
Source noteuspto-grants-2011_07