Methyl iodide → 3,5-Diallyl-4-methoxybenzoic acid methyl ester
Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:17])[C:4]1[CH:9]=[C:8]([CH2:10][CH:11]=[CH2:12])[C:7]([OH:13])=[C:6]([CH2:14][CH:15]=[CH2:16])[CH:5]=1.[CH3:18]I>>[CH3:1][O:2][C:3](=[O:17])[C:4]1[CH:9]=[C:8]([CH2:10][CH:11]=[CH2:12])[C:7]([O:13][CH3:18])=[C:6]([CH2:14][CH:15]=[CH2:16])[CH:5]=1Komponenten
3
Versuchsvorschrift
3,5-Diallyl-4-methoxybenzoic acid methyl ester was prepared from 3,5-diallyl-4-hydroxybenzoic acid methyl ester and methyl iodide following Method C. The resulting product was used without further purification.
Aufarbeitung
- customThe resulting product was used without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-ff0f3e710cec4dcdbf0bc29401920947
- Quelldatensatz
- uspto-grants-2010_04
- Patentnummer
- US07691843B2
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