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O-Phenylenediamine → o-Oleoylaminoaniline

HRID 892876
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인쇄 미리보기

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HRID 892876 반응식
C1(N=C=NC2CCCCC2)CCCCC1.[C:16]([OH:35])(=O)[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]/[CH:24]=[CH:25]\[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33].[C:36]1([NH2:43])[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=1[NH2:42]>C(Cl)Cl>[C:16]([NH:42][C:37]1[CH:38]=[CH:39][CH:40]=[CH:41][C:36]=1[NH2:43])(=[O:35])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]/[CH:24]=[CH:25]\[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7243O-PhenylenediamineHCID 10868DicyclohexylcarbodiimideHCID 445639Oleic Acid

생성물 1

HCID 42604663o-Oleoylaminoaniline수율 76.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

N,N'-Dicyclohexylcarbodiimide (2.27 g) was added to a solution of 2.82 g of oleic acid and 1.62 g of o-phenylenediamine in 50 ml of methylene chloride with stirring under ice cooling. The mixture was stirred at room temperature for one night. After completion of the reaction insoluble matter was filtered, followed by removal of the solvent by evaporation. The residue obtained was purified by silica gel column chromatography to obtain 2.84 g of the objective compound (yield: 76%).

후처리

  1. stirringThe mixture was stirred at room temperature for one night
  2. filtrationAfter completion of the reaction insoluble matter was filtered
  3. customfollowed by removal of the solvent by evaporation
  4. customThe residue obtained
  5. customwas purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-113d875ef41f40b19c7720443b250126
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05120738

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