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Azobisisobutyronitrile → HCID 86759231, 화합물

HRID 478920
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HRID 478920 반응식
[C:1]12([C:11]3([C:21]([O-:23])=[O:22])[CH2:16][CH:15]4[CH2:17][C:12]3([CH:18]([CH3:20])[CH3:19])[CH:13]=[CH:14]4)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[C:24]1(=[O:30])[O:29][C:27](=[O:28])[CH:26]=[CH:25]1.CC(N=NC(C#N)(C)C)(C#N)C>C1COCC1>[C:1]12([C:11]3([C:21]([O-:23])=[O:22])[CH2:16][CH:15]4[CH2:17][C:12]3([CH:18]([CH3:20])[CH3:19])[CH:13]=[CH:14]4)[CH2:2][CH:3]3[CH2:9][CH:7]([CH2:6][CH:5]([CH2:4]3)[CH2:10]1)[CH2:8]2.[C:27]1(=[O:28])[O:29][C:24](=[O:30])[CH:25]=[CH:26]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 7923Maleic AnhydrideHCID 86759232HCID 86759232, 화합물

생성물 1

HCID 86759231HCID 86759231, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

10.8 g of 1-adamantyl-1-methylethyl-5-norbornene-2-carboxylate prepared in Example 1, and 3.37 g of maleic anhydride were dissolved in 7.1 9 of THF. 0.112 g of AIBN was added to the resultant, degassed and polymerized at a temperature of about 65° C. for about 24 hours.

후처리

  1. customdegassed
  2. custompolymerized at a temperature of about 65° C. for about 24 hours

출처 및 근거

ORD 기록
ord-fc1fcef7da60443da07a59caf901c296
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06642336B1

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