Water → 2-Triphenylphosphoranylidene-1,4-butanedioic Acid
Reaction equation
[C:1]1([P:7]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[C:8]2[CH2:12][C:11](=[O:13])[O:10][C:9]2=[O:14])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH2:27]>>[C:21]1([P:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)=[C:8]([CH2:12][C:11]([OH:10])=[O:13])[C:9]([OH:14])=[O:27])[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1Participants
3
Procedure
The title compound was prepared by stirring 3-triphenylphosphoranylidene dihydro-2,5-furandione (5.0 g, 0.014 mole) for 48 hours in 100 ml water. The solid residue was isolated by filtration and air-dried to give essentially quantitative yields of a product as a white crystalline solid whose IR spectrum and elemental analysis corresponded to the structure ##STR8##
Workup
- customThe solid residue was isolated by filtration
- customair-dried
- customto give essentially quantitative
Sources & evidence
- ORD record
- ord-cc449d1efdd84ce081baf31c4066cc3e
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04131633
Reaction notes
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