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O-Phenylenediamine → o-Oleoylaminoaniline

HRID 892876
ノート
印刷プレビュー

反応式

HRID 892876 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7243O-PhenylenediamineHCID 10868DicyclohexylcarbodiimideHCID 445639Oleic Acid

生成物 1

HCID 42604663o-Oleoylaminoaniline収率 76.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-113d875ef41f40b19c7720443b250126
出典データセット
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05120738

反応ノート

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