Titanium tetrabutoxide → HCID 131731079, compound

HRID 1911721Notes

Reaction equation

HRID 1911721 reaction equation
[CH2:1]([P:3]([CH2:6][CH:7]([CH3:10])[CH2:8][OH:9])(=[O:5])[OH:4])[CH3:2].[O-]CCCC.[O-]CCCC.[O-]CCCC.[O-]CCCC.[Ti+4:31]>C1(C)C=CC=CC=1>[Ti+4:31].[CH2:1]([P:3]([CH2:6][CH:7]([CH3:10])[CH2:8][OH:9])(=[O:4])[O-:5])[CH3:2].[CH2:1]([P:3]([CH2:6][CH:7]([CH3:10])[CH2:8][OH:9])(=[O:4])[O-:5])[CH3:2].[CH2:1]([P:3]([CH2:6][CH:7]([CH3:10])[CH2:8][OH:9])(=[O:4])[O-:5])[CH3:2].[CH2:1]([P:3]([CH2:6][CH:7]([CH3:10])[CH2:8][OH:9])(=[O:4])[O-:5])[CH3:2]

Participants

4

Procedure

166 g (1 mol) of ethyl(2-methyl-3-hydroxypropyl)phosphinic acid (produced as in Example 13) and 85 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 161 g (91% of theory) of ethyl(2-methyl-3-hydroxypropyl)phosphinic 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-dc54707720304c87b2c631a1a55cd410
Source dataset
uspto-grants-2013_12
Patent number
US08604108B2

Reaction notes

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