Hydroxyamine hydrochloride → HCID 86753372, Verbindung
Reaktionsgleichung
[C:1]([C:3]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:4]=1[CH2:5][CH2:6][C:7]2=O)#[N:2].Cl.[NH2:14][OH:15]>C(O)C>[C:1]([C:3]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:4]=1[CH2:5][CH2:6][C:7]2=[N:14][OH:15])#[N:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
A mixture of 157 mg (1.0 mmol) of 4-cyano-2,3-dihydro-1H-inden-1-one [Coll. Czechoslov. Chem. Commun. 43, 3227 (1978)] and 139 mg (2.0 mmol) of hydroxylamine hydrochloride in 4 ml of ethanol is stirred at 80° C. for 1.5 hours and cooled in an ice-water bath. The product that has crystallized out is filtered off with suction, washed with cold ethanol and diethyl ether and dried. In that manner there is obtained the intermediate 4-cyano-2,3-dihydro-1H-inden-1-one oxime, which melts at 200°-202° C. with decomposition; 1H-NMR (DMSO): δ=11.22 (s, 1H); 7.84 (d, 1H); 7.81 (d, 1H); 7.45 (t, 1H); 3.15 (t, 2H); 2.84 (t, 2H).
Aufarbeitung
- temperaturecooled in an ice-water bath
- customThe product that has crystallized out
- filtrationis filtered off with suction
- washwashed with cold ethanol and diethyl ether
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-7aac53a229bc4825a1d4c8d8b18f7866
- Quelldatensatz
- uspto-grants-1998_11
- Patentnummer
- US05840911
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