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Phenol → Trihexyl borate

HRID 1613121
Notes
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Reaction equation

HRID 1613121 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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 996PhenolHCID 78412Phenyl dihydrogen orthoborateHCID 14178740Methylborat

Product 1

HCID 21423Trihexyl borate

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

  1. customReaction
  2. 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
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05192650

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes