Hydrochloric Acid → Tri-n-butyl(1,2-dicarboxyethyl)phosphonium Chloride
Reaction equation
[O:1]1C=CC(=O)C1=O.[CH2:8]([P:12]([CH2:24][CH2:25][CH2:26][CH3:27])([CH2:20][CH2:21][CH2:22][CH3:23])=[C:13]1[CH2:17][C:16](=[O:18])[O:15][C:14]1=[O:19])[CH2:9][CH2:10][CH3:11].[ClH:28]>O>[Cl-:28].[CH2:8]([P+:12]([CH2:24][CH2:25][CH2:26][CH3:27])([CH2:20][CH2:21][CH2:22][CH3:23])[CH:13]([C:14]([OH:1])=[O:19])[CH2:17][C:16]([OH:15])=[O:18])[CH2:9][CH2:10][CH3:11]Participants
5
Procedure
The title compound was prepared and identified by the procedures in Example 12 except that the furandione reactant here used was the tri-n-butylphosphoranylidene dihydro-2,5-furandione from Example 1 and HCl was used in place of HBr. It too was a water-soluble white crystalline solid.
Sources & evidence
- ORD record
- ord-23f9212e55194a3aa887da271bb18b16
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04131633
Reaction notes
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