Acetic Acid → 6-(tert-butyl)phthalazin-1(2H)-one
Reaktionsgleichung
[C:1]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[C:10](=O)[O:9][CH:8]2OCC)([CH3:4])([CH3:3])[CH3:2].O.[NH2:19][NH2:20].C(O)(=O)C>O>[C:1]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[C:10](=[O:9])[NH:20][N:19]=[CH:8]2)([CH3:4])([CH3:3])[CH3:2]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2.9 g (12 mmol) of 5-tert-butyl-3-ethoxy-3H-isobenzofuran-1-one was weighed into a 50 mL round bottom flask fitted with a stir bar and cap. Added 10 mL (130 mmol) of hydrazine monohydrate. Added 15 mL of glacial acetic acid. Stirred at 100° overnight. Poured the reaction mixture into 200 mL of stirred water. Collected the solids by filtration and washed with water. Dried under high vacuum to obtain 2.24 g of the title compound as an off-white solid. MS (ESI) 203 (M+H)+.
Aufarbeitung
- customfitted with a stir bar
- customcap
- customCollected the solids
- filtrationby filtration
- washwashed with water
- customDried under high vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-68cd45bbe99542db8bd02fc15ddb4dbd
- Quelldatensatz
- uspto-grants-2013_12
- Patentnummer
- US08618098B2
Notizen zur Reaktion
Wird geladen…