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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736850Generated: October 25, 2026

Water → 2-Methoxy-3,5-heptanedione

https://huagongshe.com/reaction/736850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantPropanoic acid, 2-methoxy-, methyl esterHCID 86599—
ReactantPotassium tert-butoxideHCID 23665647—
SolventAcetic AcidHCID 176—
Product2-Methoxy-3,5-heptanedioneHCID 2498713162%

Reaction Conditions

Temperature10 °C

Reaction Steps

In a 200 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel was placed 25.0 g (223 mmol) of potassium t-butoxide, and the flask was purged with argon. Then, 100 mL of methylcyclohexanone was placed in the flask. Subsequently, 12.5 g (106 mmol) of methyl 2-methoxypropionate (prepared by the method of Reference Example 1) was dropped under cooling with ice, and further 7.70 g (107 mmol) of 2-butanone was slowly dropped. The mixture was cooled to 10° C. and stirred for 30 minutes for carrying out a reaction. After the reaction was complete, 70 mL of water was placed in the flask under cooling with ice. The aqueous portion was taken out, neutralized with acetic acid, and subjected to extraction with methylcyclohexane. The methylcyclohexane extract was washed with water, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated and distilled under reduced pressure (77° C., 1.26 kPa) to give 10.4 g (yield: 62%) of 2-methoxy-3,5-heptanedione as colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595414B2
Source datasetuspto-grants-2009_09
ORD IDord-1dc7f19806e74dc8875e4596a52c86c4
Source noteuspto-grants-2009_09