Propionic Acid → Dimethyl (3,3-dimethyl-2-oxo-4-phenylbutyl)phosphonate
Reaktionsgleichung
[C:1](O)(=O)C(C)C.C(O)(=O)CC.[CH3:12][CH:13]([CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[C:14](=[O:22])[CH2:15][P:16](=[O:21])([O:19][CH3:20])[O:17][CH3:18].C(Cl)C1C=CC=CC=1>>[CH3:12][C:13]([CH3:1])([CH2:23][C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)[C:14](=[O:22])[CH2:15][P:16](=[O:21])([O:19][CH3:20])[O:17][CH3:18]Komponenten
5
Versuchsvorschrift
Further, following the procedure of Preparation 1, but using in place of the isobutyric acid of Preparation 1, part A, propionic acid, there is prepared dimethyl 3-methyl-2-oxo-4-phenylbutylphosphonate. Following the procedure of Preparation 1, but using the substituted benzyl chlorides described above in place of benzyl chloride and propionic acid in place of isobutyric acid there are prepared the various dimethyl 3-methyl-2-oxo-4-(substituted phenyl)-butylphosphonates wherein the phenyl substitution is as described above.
Aufarbeitung
- customthe procedure of Preparation 1
- customthe procedure of Preparation 1
Quellen und Nachweise
- ORD-Eintrag
- ord-ee80e715f6424a898fe58ecae6fcc2f4
- Quelldatensatz
- uspto-grants-1978_10
- Patentnummer
- US04122282
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