1,3-Diisopropylbenzene → Bis(1-methylethyl)benzene

HRID 1700872

반응식

HRID 1700872 반응식
C(C1C=CC=C(C(C)C)C=1)(C)C.[O-]O.C(C1C=CC=C(C(C)C)C=1)(C)C.[OH-].[Na+].[O-]O.[O-]O.[CH:33]([C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=1[CH:42]([CH3:44])[CH3:43])([CH3:35])[CH3:34].[O-]O.[O-]O.C(C1C=CC=C(C(C)C)C=1)(C)C.OOO.C(C1C=CC=C(C(C)C)C=1)(C)C>>[CH:42]([C:37]1[CH:38]=[CH:39][CH:40]=[CH:41][C:36]=1[CH:33]([CH3:35])[CH3:34])([CH3:44])[CH3:43]

참가 물질

8

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온도
90 °C

실험 절차

Three hundred parts of m-diisopropylbenzene (m-DIPB) were mixed with 30 parts of m-diisopropylbenzene monohydroperoxide (MHP; initiator) and 10 parts of 4% aqueous sodium hydroxide (catalyst) in a 1 liter Parr reactor and oxidized by passing air at the rate of 20 liters/hour with good agitation. The temperature of the oxidation reaction mixture was maintained at about 90° C. The oxidation was continued until the product contained 70 to 75% hydroperoxide (determined by the iodimetric titration and calculated as diisopropylbenzene monohydroperoxide). NMR analysis of this oxidation material (oxidate) showed the presence of about 15-18% m-diisopropylbenzene dihydroperoxide (DHP) and 3 to 5% m-diisopropylbenzene hydroxyhydroperoxide (HHP) in addition to the oxidation by-products shown in Table 1, below, and unreacted DIPB.

후처리

  1. customThe temperature of the oxidation reaction mixture
  2. additionin addition to the oxidation by-products

출처 및 근거

ORD 기록
ord-df00e4bd70b242c18760a78bfed62ae3
출처 데이터셋
uspto-grants-2002_02
특허 번호
US06350921B1

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