Titanium tetrabutoxide → 2-(Ethylhydroxyphosphinyl)acetic acid titanium salt

HRID 878928Notes

Reaction equation

HRID 878928 reaction equation
[CH2:1]([P:3]([OH:9])([CH2:5][C:6]([OH:8])=[O:7])=[O:4])[CH3:2].[O-]CCCC.[O-]CCCC.[O-]CCCC.[O-]CCCC.[Ti+4:30]>C1(C)C=CC=CC=1>[Ti+4:30].[CH2:1]([P:3]([OH:9])([CH2:5][C:6]([O-:8])=[O:7])=[O:4])[CH3:2].[CH2:1]([P:3]([CH2:5][C:6]([O-:8])=[O:7])([OH:9])=[O:4])[CH3:2].[CH2:1]([P:3]([CH2:5][C:6]([O-:8])=[O:7])([OH:9])=[O:4])[CH3:2].[CH2:1]([P:3]([CH2:5][C:6]([O-:8])=[O:7])([OH:9])=[O:4])[CH3:2]

Participants

4

Procedure

152 g (1 mol) of 2-(ethylhydroxyphosphinyl)acetic acid (produced as in Example 10) 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.

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-5850a620a4144615b4d627f3b8d56a47
Source dataset
uspto-grants-2015_03
Patent number
US08987489B2

Reaction notes

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