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

HRID 1526931Notes

Reaction equation

HRID 1526931 reaction equation
[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]

Participants

4

Procedure

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.

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-19f7154903b545a7ab27ad15880aa3ce
Source dataset
uspto-grants-2015_07
Patent number
US09085734B2

Reaction notes

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