Titanium tetrabutoxide → HCID 131731098, compound
Reaction equation
[CH2:1]([P:3]([CH2:6][CH:7](C)[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][CH2:7][CH2:8][OH:9])(=[O:4])[O-:5])[CH3:2].[CH2:1]([P:3]([CH2:6][CH2:7][CH2:8][OH:9])(=[O:4])[O-:5])[CH3:2].[CH2:1]([P:3]([CH2:6][CH2:7][CH2:8][OH:9])(=[O:4])[O-:5])[CH3:2].[CH2:1]([P:3]([CH2:6][CH2:7][CH2:8][OH:9])(=[O:4])[O-:5])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
166 g (1 mol) of ethyl(2-methyl-3-hydroxypropyl)phosphinic acid (produced as in Example 5) 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(3-hydroxypropyl)phosphinic acid titanium salt.
Workup
- distillationThe resulting butanol is distilled off from time to time with proportions of toluene
- customThe solution formed
Sources & evidence
- ORD record
- ord-c1a50d46b5324158944b2c153da31777
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08614267B2
Reaction notes
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