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

HRID 1028265Notes

Reaction equation

HRID 1028265 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 11) 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-8f6100a9796a414db6d6bff8b99b3c7e
Source dataset
uspto-grants-2014_05
Patent number
US08735476B2

Reaction notes

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