HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19116Generated: October 30, 2026
Ethyl 2-butynoate → HCID 66893867, compound
https://huagongshe.com/reaction/19116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-butynoate | HCID 78043 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-Ethoxy-2,6-difluorophenol | HCID 55275768 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66893867 | HCID 66893867 | 67.4% |
Reaction Steps
To a stirred mixture of 3-ethoxy-2,6-difluoro-phenol (4.26 g, 0.024 mol) and ethyl-2-butynoate (5.48 g, 0.049 mol) in tetrahydrofuran (30 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (3.73 g, 0.025 mol) slowly. After addition was complete the mixture was stirred at reflux for 6 h. Upon completion of the reaction the tetrahydrofuran was removed in vacuo and the residue was diluted in diethyl ether and washed first with 1N aqueous hydrochloric acid, then 10% aqueous sodium hydroxide solution, a saturated sodium chloride solution and dried over magnesium sulfate. The crude product was purified by ISCO column chromatography (Teledyne Isco RediSep Flash Column 120 g, 0% to 20% ethyl acetate/hexanes) which afforded (E)-3-(3-ethoxy-2,6-difluoro-phenoxy)-but-2-enoic acid ethyl ester (4.63 g, 66%) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741327B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-d69bc81208024a4dba05f317e3bcac65 |
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| Source note | uspto-grants-2010_06 |
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