Phenol → BPTMC phenol

HRID 488543

반응식

HRID 488543 반응식
[CH3:1][CH:2]1[CH2:7][C:6]([C:15]2[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=2)([C:8]2[CH:13]=[CH:12][C:11]([OH:14])=[CH:10][CH:9]=2)[CH2:5][C:4]([CH3:23])([CH3:22])[CH2:3]1.[C:24]1([OH:30])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.CC1(C)CC(C)CCC1>>[CH3:1][CH:2]1[CH2:7][C:6]([C:8]2[CH:9]=[CH:10][C:11]([OH:14])=[CH:12][CH:13]=2)([C:15]2[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=2)[CH2:5][C:4]([CH3:22])([CH3:23])[CH2:3]1.[C:24]1([OH:30])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

참가 물질

4

실험 절차

In the present invention, the solution comprising BPTMC and phenol can be any solution containing BPTMC and phenol and is not particularly limited, but preferably an oil phase containing BPTMC and phenol, which is obtained by reacting phenol and 3,3,5-trimethylcyclohexane in the presence of an acid catalyst, neutralizing the resulting reaction mixture after completion of the reaction and then removing a water phase; this water phase is cooled to crystallize the BPTMC-phenol adduct and the crystallized BPTMC-phenol adduct (phenol adduct crystal) is isolated, for example, by filtration to obtain the BPTMC-phenol adduct. In this case, the resulting phenol adduct crystal generally contains isomers, high boiling point byproducts such as polymers, colored byproducts and trace impurities such as sodium, besides BPTMC and phenol. Therefore, colorless high purity BPTMC could not generally be obtained without such operations as dissolution, recrystallization and filtration of this BPTMC-phenol adduct using a solvent.

후처리

  1. customwhich is obtained
  2. customthe resulting reaction mixture
  3. customafter completion of the reaction
  4. customremoving a water phase
  5. temperaturethis water phase is cooled
  6. customto crystallize the BPTMC-phenol adduct

출처 및 근거

ORD 기록
ord-b3869861372c4621b9c618fdec447128
출처 데이터셋
uspto-grants-2005_12
특허 번호
US06972344B2

연결된 노트

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