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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20612Generated: October 26, 2026

Sulfuric Acid → 1,1,5,5-Tetramethoxypentane-3-one

https://huagongshe.com/reaction/20612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTolueneHCID 1140—
ReactantMethyl formateHCID 7865—
ReactantSodium HydroxideHCID 14798—
Reactant3-Buten-2-one, 4-methoxy-HCID 94297—
ReactantSodium MethoxideHCID 10942334—
Product1,1,5,5-Tetramethoxypentane-3-oneHCID 2314479918%

Reaction Conditions

Temperature15 °C

Reaction Steps

In a flask made of glass having an inner volume of 500 ml and equipped with a stirring device and a dropping funnel were charged 37 g (0.68 mol) of sodium methoxide and 200 ml of toluene, and while maintaining the liquid temperature to 15° C. or lower, a mixed solution comprising 50 g (0.50 mol) of 1-methoxy-1-buten-3-one and 60 g (1.0 mol) of methyl formate was gently added dropwise to the mixture. After completion of the dropwise addition, the mixture was reacted at 15° C. or lower for 1 hour, and at room temperature for 3 hours. Thereafter, the reaction solution was concentrated under reduced pressure, 50 ml of methanol was added to the concentrate, 60 g (0.6 mol) of 98% sulfuric acid was gently added dropwise to the mixture while maintaining the liquid temperature to 15° C. or lower, and the mixture was reacted under stirring at room temperature for 5 hours. After completion of the reaction, 50% aqueous sodium hydroxide solution was added to the mixture to neutralize the same, the precipitated solid was filtered off, and the obtained filtrate was concentrated. The concentrate was purified by silica gel column chromatography (Eluent; hexane:ethyl acetate=10:1) to give 18.5 g (Isolation yield: 18%) of 1,1,5,5-tetramethoxypentane-3-one as orange liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745649B2
Source datasetuspto-grants-2010_06
ORD IDord-796ff46e6d6c44dc939b94753c106143
Source noteuspto-grants-2010_06