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Phenyl isocyanate → 1-Phenyl-3-[2-(3-isopropenylphenyl)-2-propyl]carbodiimide

HRID 1707222
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인쇄 미리보기

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HRID 1707222 반응식
CC1CCP(=O)(C2C=CC=CC=2)C=1.[CH3:14][C:15]([C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([N:26]=[C:27]=O)([CH3:25])[CH3:24])[CH:18]=1)=[CH2:16].[C:29]1([N:35]=C=O)[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.C1(N=C=NC2C=CC=CC=2)C=CC=CC=1>>[C:29]1([N:35]=[C:27]=[N:26][C:23]([C:19]2[CH:20]=[CH:21][CH:22]=[C:17]([C:15]([CH3:14])=[CH2:16])[CH:18]=2)([CH3:25])[CH3:24])[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 7672Phenyl isocyanateHCID 697221H-Phosphole, 2,3-dihydro-4-methyl-1-phenyl-, 1-oxideHCID 98693N,N'-Methanetetraylbis(benzenamine)HCID 6041521-(1-Isocyanato-1-methylethyl)-3-(1-methylethenyl)benzene

생성물 1

HCID 231929181-Phenyl-3-[2-(3-isopropenylphenyl)-2-propyl]carbodiimide

실험 절차

We combined 0.3182 g 3-methyl-l-phenyl-2-phospholene-1-oxide (MPPO), m-TMI [2-(3-isopropenylphenyl)-2-propylisocyanate], and 19.31 g phenyl isocyanate. After heating at 140°-150° C. for 14 hours, IR showed nearly complete conversion of isocyanates to carbodiimides. GC-MS integrated ionization current shows a response of 265944 units for the title mixed product, 3558 units for the diphenyl carbodiimide, and 3602 units for the ditertiarycarbodiimide. Assuming that the detector sensitivity for the mixed product is the same, the selectivity for the mixed product is the average of the two other products, the reaction selectivity for the mixed product is 265944/(265944+3602+3558) or 97%, so the maximum yield of either mixed product is 3%.

후처리

  1. temperatureAfter heating at 140°-150° C. for 14 hours

출처 및 근거

ORD 기록
ord-4d4b7bbd12c34427b3fe448dbfb5d803
출처 데이터셋
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05352400

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