Titanium tetrabutoxide → 3-(Ethylhydroxyphosphinyl)-2-methylpropionic acid titanium salt

HRID 1028260Notes

Reaction equation

HRID 1028260 reaction equation
[CH2:1]([P:3]([OH:11])([CH2:5][CH:6]([CH3:10])[C:7]([OH:9])=[O:8])=[O:4])[CH3:2].[O-]CCCC.[O-]CCCC.[O-]CCCC.[O-]CCCC.[Ti+4:32]>C1(C)C=CC=CC=1>[Ti+4:32].[CH2:1]([P:3]([OH:11])([CH2:5][CH:6]([CH3:10])[C:7]([O-:9])=[O:8])=[O:4])[CH3:2].[CH2:1]([P:3]([CH2:5][CH:6]([CH3:10])[C:7]([O-:9])=[O:8])([OH:11])=[O:4])[CH3:2].[CH2:1]([P:3]([CH2:5][CH:6]([CH3:10])[C:7]([O-:9])=[O:8])([OH:11])=[O:4])[CH3:2].[CH2:1]([P:3]([CH2:5][CH:6]([CH3:10])[C:7]([O-:9])=[O:8])([OH:11])=[O:4])[CH3:2]

Participants

4

Procedure

180 g (1 mol) of 3-(ethylhydroxyphosphinyl)-2-methylpropionic acid (produced as in Example 17) 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 184 g (91% of theory) of 3-(ethylhydroxyphosphinyl)-2-methylpropionic acid titanium salt.

Workup

  1. distillationThe resulting butanol is distilled off from time to time with proportions of toluene
  2. customThe solution formed

Sources & evidence

ORD record
ord-c9faf8190bf74c4dbc43fb572a816389
Source dataset
uspto-grants-2014_05
Patent number
US08735477B2

Reaction notes

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