Reaktionsgleichung
[C:1]1([CH:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[C:9](=O)[CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CO.C(=O)([O-])[O-].[K+].[K+].Cl.[NH2:26][OH:27]>O>[OH:27][N:26]=[C:9]1[C:10]2[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[CH2:8]1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 3-phenylindan-1-one (80 g), methanol (935 ml), water (90 ml), potassium carbonate (103.8 g), and hydroxylamine HCl (104.3 g) was heated at reflux for 16 hours, then poured into ice-water: the title compound was filtered, washed with water, with a small portion of ether, then dried in air. Yield: 74.7 g; m.p. 133°-139°.
Aufarbeitung
- temperaturewas heated
- temperatureat reflux for 16 hours
- filtrationthe title compound was filtered
- washwashed with water, with a small portion of ether
- customdried in air
Quellen und Nachweise
- ORD-Eintrag
- ord-06804961a4a94f6fab538831a07fec43
- Quelldatensatz
- uspto-grants-1985_10
- Patentnummer
- US04548946
Verknüpfte Notizen
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