Bis(4-hydroxyphenyl)methane → 1,1'-(Methylenedi-p-phenylene)bismaleimide

HRID 1893067

반응식

HRID 1893067 반응식
[CH:1]1[C:6]([CH2:7][C:8]2[CH:9]=[CH:10][C:11](O)=[CH:12][CH:13]=2)=[CH:5][CH:4]=[C:3](O)[CH:2]=1.CC1C([N:26]2[C:30](=[O:31])[CH:29]=[CH:28][C:27]2=[O:32])=C(C=CC=1)C(Cl)=O>C(N(CC)CC)C.ClCCCl>[CH:1]1[C:6]([CH2:7][C:8]2[CH:9]=[CH:10][C:11]([N:26]3[C:30](=[O:31])[CH:29]=[CH:28][C:27]3=[O:32])=[CH:12][CH:13]=2)=[CH:5][CH:4]=[C:3]([N:26]2[C:27](=[O:32])[CH:28]=[CH:29][C:30]2=[O:31])[CH:2]=1

참가 물질

5

실험 절차

A 6.0 g quantity of 4,4′-dihydroxydiphenylmethane is dissolved in a solution of 12.6 ml of triethylamine in 50 ml of 1,2-dichloroethane in a 250 ml flask. To the solution is slowly added a solution of 15.5 g of methyl maleimidobenzoyl chloride in 50 ml of 1,2-dichloroethane. The mixture is allowed to react at room temperature for 16 hr. The reaction mixture is precipitated in water, filtered under reduced pressure, washed sequentially with water and ethanol, and dried at 60° C. under vacuum for 48 hr, yielding the bismaleimide compound of Formula 20m.

후처리

  1. customto react at room temperature for 16 hr
  2. customThe reaction mixture is precipitated in water
  3. filtrationfiltered under reduced pressure
  4. washwashed sequentially with water and ethanol
  5. customdried at 60° C. under vacuum for 48 hr

출처 및 근거

ORD 기록
ord-0b52e23c04354260b8fc09e02c6e2208
출처 데이터셋
uspto-grants-2013_08
특허 번호
US08512596B2

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