참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,3-Diisopropylbenzene | HCID 7450 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Perhydroxyl radical | HCID 18500 | — |
| 반응물 | m-Diisopropylbenzene hydroxyhydroperoxide | HCID 18319342 | — |
| 반응물 | Hydroperoxide,1,1'-[1,3-phenylenebis(1-methylethylidene)]bis- | HCID 53471113 | — |
| 반응물 | Diisopropyl benzene hydroperoxide | HCID 57376481 | — |
| 반응물 | m-Diisopropylbenzene monohydroperoxide | HCID 71436539 | — |
| 생성물 | Bis(1-methylethyl)benzene | HCID 11345 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06350921B1 |
|---|
| 출처 데이터셋 | uspto-grants-2002_02 |
|---|
| ORD ID | ord-df00e4bd70b242c18760a78bfed62ae3 |
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| 출처 메모 | uspto-grants-2002_02 |
|---|
