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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370678Generated: November 3, 2026

Dimethyl Sulfate → Ethyl (2Z)-2-(ethoxymethyl)-3-methoxyprop-2-enoate

https://huagongshe.com/reaction/2370678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantEthyl formateHCID 8025—
ReactantHexaneHCID 8058—
ReactantSodium HydroxideHCID 14798—
ReactantTriethylazanium chlorideHCID 12698378—
ProductEthyl (2Z)-2-(ethoxymethyl)-3-methoxyprop-2-enoateHCID 5348675837%

Reaction Conditions

Temperature50 °C

Reaction Steps

Sodium (40.9 g, 1.78 mol) was added to ethanol (750 mL) in portions carefully and the solution was concentrated to give NaOEt powder after all sodium metal disappeared. Under stirring, hexane (1.0 L) was added and the mixture was cooled with ice-water bath. A mixture of 201 (130 g, 0.89 mol) and ethyl formate (131 g, 1.78 mol) was added dropwise at 0-5° C. The reaction mixture was stirred at room temperature overnight. Dimethyl sulfate (224 g, 1.78 mol) was added dropwise with cooling of ice-water bath. The resulting mixture was heated at 50° C. for 2 h. To the mixture was added triethylammonium chloride (122 g) and sodium hydroxide (20 g). The mixture was then stirred at room temperature for 4 h and filtered. The filtrate was washed with water and dried over Na2SO4. It was concentrated to afford the titled compound (140 g, 37%) as a colorless oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710219B2
Source datasetuspto-grants-2014_04
ORD IDord-c7e77f734f3b43b49c7ace927510e7f4
Source noteuspto-grants-2014_04