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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297695Generated: November 1, 2026

Acetic Anhydride → Ethyl 3-ethoxy-2-(methanesulfonyl)prop-2-enoate

https://huagongshe.com/reaction/1297695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
ReactantEthyl methanesulfonylacetateHCID 78201—
ProductEthyl 3-ethoxy-2-(methanesulfonyl)prop-2-enoateHCID 71353473—

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of methanesulfonyl-acetic acid ethyl ester (example 61b) (90 g, 0.547 mol), triethyl orthoformate (242.9 g, 0.641 mol), and acetic anhydride (227 mL) was heated at 130-140° C. for three hours. After cooling the reaction to room temperature, solvent was removed under reduced pressure to give 3-ethoxy-2-methanesulfonyl-acrylic acid ethyl ester (purity 50%). The crude compound was used in the following reaction without further purification. LC-MS m/e 223 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250515B2
Source datasetuspto-grants-2007_07
ORD IDord-72ab3f79ef514a6992d1ebec49bdff3f
Source noteuspto-grants-2007_07