Acetone → HCID 21487973, Verbindung
Reaktionsgleichung
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]3[CH:24]=[CH:23][CH:22]=[CH:21][C:11]=3[C:12]=2C2C=C(C)C=C(C)C=2)=[CH:4][CH:3]=1.[C:25](=[O:28])([O-])[O-].[K+].[K+].[CH3:31][N:32]([CH3:37])[CH2:33][CH2:34][CH2:35]Cl.[CH3:38][C:39]([CH3:41])=O>>[CH3:31][N:32]([CH3:37])[CH2:33][CH2:34][CH2:35][O:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:9][C:10]3[CH:24]=[CH:23][CH:22]=[CH:21][C:11]=3[C:12]=2[C:25](=[O:28])[C:39]2[CH:41]=[C:7]([CH3:6])[CH:2]=[C:3]([CH3:4])[CH:38]=2)=[CH:6][CH:7]=1Komponenten
5
Versuchsvorschrift
Treatment of 2-p-hydroxyphenyl-3-(3',5'-dimethylphenyl)benzofuran with potassium carbonate and 3-dimethylaminopropyl chloride in dry acetone by the procedure described in Example 31 gave the title compound.
Quellen und Nachweise
- ORD-Eintrag
- ord-5994e338e9d54d69b413a13d76c1352d
- Quelldatensatz
- uspto-grants-1977_01
- Patentnummer
- US04001426
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