Reaktionsgleichung
Cl.[C:2]([NH:6][NH2:7])([CH3:5])([CH3:4])[CH3:3].Cl.[C:9]([C:17](O)=[O:18])(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>O>[C:2]([NH:6][N:7]=[C:17]([C:9](=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[OH:18])([CH3:5])([CH3:4])[CH3:3]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 296 grams (g) (2.37 mol) of t-butyl hydrazine hydrochloride, 20 milliliters (mL) of concentrated hydrochloric acid (HCl) and 2 liters (L) of water was stirred at room temperature to give a clear solution. Benzoylformic acid (400 g, 2.61 mol) was added in four equal portions at 3 minute intervals. The mixture was stirred overnight at room temperature and filtered. The solid collected was washed with water and dried in vacuo to furnish 520 g (99%) of the compound, mp 138°-139° C.
Aufarbeitung
- customto give a clear solution
- stirringThe mixture was stirred overnight at room temperature
- filtrationfiltered
- customThe solid collected
- washwas washed with water
- customdried in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-9e10897343474022a906743422cbf754
- Quelldatensatz
- uspto-grants-1994_08
- Patentnummer
- US05334726
Verknüpfte Notizen
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