Phenol → Trihexyl borate
Reaction equation
[C:1]1(OB(O)O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:11][O:12][B:13]([OH:15])[OH:14].[C:16]1(O)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[B:13]([O:15][CH2:1][CH2:6][CH2:5][CH2:4][CH2:3][CH3:2])([O:14][CH2:16][CH2:21][CH2:20][CH2:19][CH2:18][CH3:17])[O:12][CH2:11][CH2:3][CH2:2][CH2:1][CH2:6][CH3:5]Participants
4
Procedure
Reaction is conducted in the same manner as described above except that phenylboric acid or methylboric acid is used instead of boric acid in the above example and a corresponding alcohol or phenol is used instead of hexyl alcohol, and then, the solvent is concentrated under reduced pressure, followed by distillation or crystallization and recrystallization with an appropriate solvent, whereby a corresponding boron compound can be obtained.
Workup
- customReaction
- concentrationthe solvent is concentrated under reduced pressure
- distillationfollowed by distillation or crystallization and recrystallization with an appropriate solvent, whereby a corresponding boron compound
- customcan be obtained
Sources & evidence
- ORD record
- ord-e7e8e5e7ab61454aa33954f41c1a59fd
- Source dataset
- uspto-grants-1993_03
- Patent number
- US05192650
Reaction notes
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