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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18700Generated: October 25, 2026

Potassium Iodide → methyl 4-acetyltetrahydro-2H-pyran-4-carboxylate

https://huagongshe.com/reaction/18700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl acetoacetateHCID 7757—
ReactantBis(2-chloroethyl) etherHCID 8115—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productmethyl 4-acetyltetrahydro-2H-pyran-4-carboxylateHCID 996427951%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a flask made of glass having an inner volume of 1000 ml and equipped with a stirring device, a thermometer, a dropping funnel and a reflux condenser were charged 143 g (1.0 mol) of 2,2′-dichloroethyl ether, 276 g (2.0 mol) of anhydrous potassium carbonate, 10 g (0.06 mol) of potassium iodide and 600 ml of N,N-dimethylformamide, and the temperature of the mixture was raised to up to 80° C. with stirring. Then, 139 g (1.2 mol) of methyl 3-oxobutanoate was gently added dropwise to the mixture, and the mixture was reacted at the same temperature for 8 hours. After completion of the reaction, 1000 ml of water was added to the reaction mixture, and the resulting mixture was extracted three times with 600 ml of ethyl acetate. The organic layers were dried over magnesium sulfate, filtered, and the filtrate was distilled under reduced pressure (125 to 127° C., 1.3 kPa) to give 95 g (Isolation yield: 50%) of 4-acetyl-4-methoxycarbonyltetrahydropyran with a purity of 98% (areal percentage by gas chromatography) as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741497B2
Source datasetuspto-grants-2010_06
ORD IDord-f0006ac45c354b1d81928a824a00193e
Source noteuspto-grants-2010_06