Toluene → HCID 21948929, Verbindung
Reaktionsgleichung
[OH:1][CH2:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[N+:13]([O-:15])=[O:14])[N:4]=1.[C:16](OC(=O)C)(=[O:18])[CH3:17].C1(C)C=CC=CC=1.CCCCCC.C(OCC)(=O)C>N1C=CC=CC=1>[C:16]([O:1][CH2:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[N+:13]([O-:15])=[O:14])[N:4]=1)(=[O:18])[CH3:17]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution that consists of 390 mg (1.91 mmol) of 2-(hydroxymethyl)-5-nitroquinoline and 2.5 ml of acetic acid anhydride in 5.0 ml of pyridine is allowed to stir for 24 hours at room temperature. After repeated co-evaporation with toluene and subsequent chromatography on silica gel with hexane-ethyl acetate (0-100%), 410 mg (87% of theory) of the product is obtained.
Aufarbeitung
- customis obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-55c73acd04dc473fade0a1acfbd6e181
- Quelldatensatz
- uspto-grants-2008_02
- Patentnummer
- US07329753B2
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