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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Ethyl methanesulfonylacetate | HCID 78201 | — |
| Product | Ethyl 3-ethoxy-2-(methanesulfonyl)prop-2-enoate | HCID 71353473 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250515B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-72ab3f79ef514a6992d1ebec49bdff3f |
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| Source note | uspto-grants-2007_07 |
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