Glyoxal → HCID 15099950, compound
Reaction equation
[CH2:1]([PH2:4])[CH2:2][CH3:3].[CH:5]([CH:7]=[O:8])=[O:6]>O1CCCC1>[CH2:1]([P:4]1[CH:5]([OH:6])[CH:7]([OH:8])[P:4]([CH2:1][CH2:2][CH3:3])[CH:5]([OH:6])[CH:7]1[OH:8])[CH2:2][CH3:3]Participants
4
Reagents, catalysts & solvents 1
Procedure
Following the procedure of Example 1, mono-n-propylphosphine, in tetrahydrofuran, as solvent, is reacted with a 40% aqueous glyoxal solution, to give 1,4-di-n-propyl-2,3,5,6-tetrahydroxy-1,4-diphosphorinane, a solid melting at 131°-133° C.
Sources & evidence
- ORD record
- ord-4a9086e58ffb49da91792f639302de2c
- Source dataset
- uspto-grants-1992_09
- Patent number
- US05149878
Reaction notes
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