HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-butynoate → (E)-3-(3-ethoxy-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester
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-fluorophenol | HCID 66894508 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-3-(3-ethoxy-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester | HCID 66894779 | — |
Reaction Steps
To a stirred mixture of 3-ethoxy-2-fluoro-phenol (6.00 g, 0.038 mol) and ethyl-2-butynoate (8.60 g, 0.077 mol) in tetrahydrofuran (50 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (5.80 g, 0.038 mol) slowly. After addition was complete the mixture was stirred at reflux for 7 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, (E)-3-(3-ethoxy-2-fluoro-phenoxy)-but-2-enoic acid ethyl ester, was obtained as a brown oil (6.00 g, 58%) and used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741327B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-8176dc49da14495abf623ed52a166703 |
| Source note | uspto-grants-2010_06 |