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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736848Generated: October 25, 2026

Acetone → 5-Methoxyhexane-2,4-dione

https://huagongshe.com/reaction/736848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium amideHCID 24533—
ReactantPropanoic acid, 2-methoxy-, methyl esterHCID 86599—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-Methoxyhexane-2,4-dioneHCID 2498677953%

Reaction Steps

In a 200 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel was placed 10.1 g (259 mmol) of sodium amide, and the flask was purged with argon. Then, 120 mL of methylcyclohexane was placed in the flask. Subsequently, 7.40 g (127 mmol) of acetone was slowly dropped into the ice-cooled mixture in the flask, and the resulting mixture was stirred for 15 minutes. Into the flask was further dropped 15.0 g (127 mmol) of methyl 2-methoxypropionate (prepared by the method of Reference Example 1), and the mixture was stirred for 30 minutes for carrying out a reaction. After the reaction was complete, 50 mL of water was placed in the flask under cooling with ice. The aqueous portion was taken out, made acetic with acetic acid, and subjected to extraction with hexane. The hexane extract was washed with water, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated and distilled under reduced pressure (66° C., 1.38 kPa) to give 9.63 g (yield: 53%) of 2-methoxy-3,5-hexanedione as colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595414B2
Source datasetuspto-grants-2009_09
ORD IDord-d3d528aa383f468a8d67cab1ec6ede37
Source noteuspto-grants-2009_09