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1,3-Butadiene → 1-Phenyl-4-cyclohexene-1,2-dicarboxylic acid anhydride

HRID 441839
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인쇄 미리보기

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HRID 441839 반응식
[C:1]1([C:7]2[C:8]([O:10][C:11](=[O:13])[CH:12]=2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:14]=[CH:15][CH:16]=[CH2:17]>C1(C)C=CC=CC=1>[C:1]1([C:7]23[C:8](=[O:9])[O:10][C:11](=[O:13])[CH:12]2[CH2:14][CH:15]=[CH:16][CH2:17]3)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 78451,3-ButadieneHCID 99174Phenylmaleic anhydride

생성물 1

HCID 126799041-Phenyl-4-cyclohexene-1,2-dicarboxylic acid anhydride

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
100 °C

실험 절차

A mixture of α-phenyl-maleic anhydride (20 g, 0.115 moles), butadiene (40 g, 0.74 moles) and 200 ml of toluene was heated at 100° C. in a sealed bomb for 15 hrs. The toluene solution was decanted from an insoluble, polymeric material and evaporated in vacuo to yield crude 1-phenyl-4-cyclohexene-1,2-dicarboxylic acid anhydride, bp 155° (0.3 mm).

후처리

  1. customThe toluene solution was decanted from an insoluble, polymeric material
  2. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-c37bfb081e7f41c9b948d30a2b36e182
출처 데이터셋
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04042707

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