Glyoxal → HCID 15099952, compound
Reaction equation
[CH2:1]([PH2:7])[CH2:2][C:3]([CH3:6])([CH3:5])[CH3:4].[CH:8]([CH:10]=[O:11])=[O:9]>O1CCCC1>[CH2:1]([P:7]1[CH:8]([OH:9])[CH:10]([OH:11])[P:7]([CH2:1][CH2:2][C:3]([CH3:4])([CH3:6])[CH3:5])[CH:8]([OH:9])[CH:10]1[OH:11])[CH2:2][C:3]([CH3:6])([CH3:5])[CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the procedure of Example 2, mononeohexyl phosphine (200 parts) in tetrahydrofuran, is reacted with 250 parts of glyoxal and 256 parts (90% yield) of 1,4-dineohexyl-2,3,5,6-tetrahydroxy-1,4-diphosphorinane, m.p. 186°-210° C., are isolated.
Sources & evidence
- ORD record
- ord-6fc57150857a46e0ab7dace5878a7ae6
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05077437
Reaction notes
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