Titanium tetrabutoxide → 2-(Ethylhydroxyphosphinyl)acetic acid titanium salt
Reaktionsgleichung
[Na+].[CH2:2]([P:4]([OH:10])([CH2:6][C:7]([O-:9])=[O:8])=[O:5])[CH3:3].[O-]CCCC.[O-]CCCC.[O-]CCCC.[O-]CCCC.[Ti+4:31]>C1(C)C=CC=CC=1>[Ti+4:31].[CH2:2]([P:4]([OH:10])([CH2:6][C:7]([O-:9])=[O:8])=[O:5])[CH3:3].[CH2:2]([P:4]([CH2:6][C:7]([O-:9])=[O:8])([OH:10])=[O:5])[CH3:3].[CH2:2]([P:4]([CH2:6][C:7]([O-:9])=[O:8])([OH:10])=[O:5])[CH3:3].[CH2:2]([P:4]([CH2:6][C:7]([O-:9])=[O:8])([OH:10])=[O:5])[CH3:3]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
152 g (1 mol) of 2-(ethylhydroxyphosphinyl)acetic acid (prepared as in Example 12) and 170 g of titanium tetrabutoxide are refluxed in 500 ml of toluene for 40 hours. The resulting butanol is distilled off from time to time with proportions of toluene. The solution formed is subsequently freed of solvent to leave 167 g (96% of theory) of 2-(ethylhydroxyphosphinyl)acetic acid titanium salt.
Aufarbeitung
- distillationThe resulting butanol is distilled off from time to time with proportions of toluene
- customThe solution formed
Quellen und Nachweise
- ORD-Eintrag
- ord-19f7154903b545a7ab27ad15880aa3ce
- Quelldatensatz
- uspto-grants-2015_07
- Patentnummer
- US09085734B2
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