HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19152Erstellt: 23. Oktober 2026
3-Cyanophenol → (E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl ester
https://huagongshe.com/de/reaction/19152
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Cyanophenol | HCID 13394 | — |
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | Methyl but-2-ynoate | HCID 141019 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl ester | HCID 66895047 | 76% |
Reaktionsschritte
To a stirred mixture of 3-hydroxy-benzonitrile (3.30 g, 0.028 mol) and methyl-2-butynoate (5.40 g, 0.055 mol) in tetrahydrofuran (50 mL) was added 1,8-diazabicyclo[5.4.0]undec-7-ene (4.20 g, 0.028 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 mixture was filtered and evaporated and the residue dried under high vacuum which afforded (E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl ester as an oil (4.60 g, 76%) and used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741327B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-fb3e6c940794475996d3ab2a68d25e21 |
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| Quellennotiz | uspto-grants-2010_06 |
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