Anthranilic Acid → N-(3',4'-dimethoxycinnamoyl)anthranilic acid

HRID 1588960ノート

反応式

HRID 1588960 の反応式
[C:1]([OH:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[Cl-].[Mg+2].[Cl-].S(Cl)(Cl)=O.[CH3:18][O:19][C:20]1[CH:25]=[CH:24][C:23](/[CH:26]=[CH:27]/[C:28](O)=[O:29])=[CH:22][C:21]=1[O:31][CH3:32]>O.CN(C)C=O>[CH3:32][O:31][C:21]1[CH:22]=[C:23]([CH:24]=[CH:25][C:20]=1[O:19][CH3:18])[CH:26]=[CH:27][C:28]([NH:4][C:3]1[C:2](=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:1]([OH:10])=[O:9])=[O:29]

参加物

7

実験手順

Into 15 ml of dimethylformamide were dissolved with heating 1.37 g (0.01 mol) of anthranilic acid and 3.2 g of magnesium chloride (anhydrous), and the resulting solution was cooled to room temperature. To 10 ml of dimethylformamide were added in order 0.78 ml of thionyl chloride and 2.08 g (0.01 mol) of 3',4'-dimethoxycinnamic acid, during which the reaction system was stirred and cooled with ice and water. After being stirred for additional 15 minutes, the resulting mixture was added dropwise to the above solution, with stirring at room temperature. After the completion of the dropping, the reaction mixture was stirred for additional 1.5 hours, and then treated in the same manner as in Example 2. There was obtained 2.71 g (yield: 82.9%) of N-(3',4'-dimethoxycinnamoyl)-anthranilic acid. Melting point: 209°-211° C.

後処理

  1. stirringAfter being stirred for additional 15 minutes
  2. additionthe resulting mixture was added dropwise to the above solution
  3. stirringwith stirring at room temperature
  4. stirringAfter the completion of the dropping, the reaction mixture was stirred for additional 1.5 hours
  5. additiontreated in the same manner as in Example 2

出典と根拠

ORDレコード
ord-7b9d8ae3920e4c009a53d6b29acc8ddb
出典データセット
uspto-grants-1993_06
特許番号
US05223639

反応ノート

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