Methyl iodide → methyl quinoline-2-carboxylate
Reaktionsgleichung
[C:1]([OH:13])(=[O:12])[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[CH3:14]I>>[C:1]([O:13][CH3:14])(=[O:12])[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1Komponenten
3
Versuchsvorschrift
Reaction of 10.0 g of quinaldic acid with 5.4 ml of methyliodide by the method described in Example 97f) for 20 h at room temperature and purification of the crude product by FC over 80 g of silica gel (mobile phase C) gives methyl quinaldate as a white solid: Rf (50:50:6 mixture of hexane, ethyl acetate and glacial acetic acid)=0.65.
Aufarbeitung
- customfor 20 h
- customat room temperature
- custompurification of the crude product by FC over 80 g of silica gel (mobile phase C)
Quellen und Nachweise
- ORD-Eintrag
- ord-5d7d138d003244b081a80983a7f8f1b6
- Quelldatensatz
- uspto-grants-1998_02
- Patentnummer
- US05719141
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