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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Triethylazanium chloride | HCID 12698378 | — |
| Product | Ethyl (2Z)-2-(ethoxymethyl)-3-methoxyprop-2-enoate | HCID 53486758 | 37% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710219B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-c7e77f734f3b43b49c7ace927510e7f4 |
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| Source note | uspto-grants-2014_04 |
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