Benzoyl chloride → HCID 20201043、化合物

HRID 978957ノート

反応式

HRID 978957 の反応式
[O:1]=[C:2]1[C:6]2[C:7]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[N:8][C:9](=[O:10])[C:5]=2[C:4]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:3]1.[C:23](Cl)(=[O:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[O:10]=[C:9]1[C:5]2=[C:4]([C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)[N:3]([C:23](=[O:30])[C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[C:2](=[O:1])[C:6]2=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[N:8]1[C:23](=[O:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

参加物

3

反応物 2

HCID 7412Benzoyl chlorideHCID 152175761,4-Dioxo-3,6-diphenylpyrrolo[3,4-c]pyrrole

生成物 1

HCID 20201043HCID 20201043、化合物

実験手順

5.8 Parts of 1,4-diketo-3,6-diphenylpyrrolo-[3,4-c]-pyrrole are stirred with 50 parts of benzoyl chloride at 190° C. for 22 hours. The starting material dissolves in the course of the reaction. On cooling of the reaction mixture, most of the reaction product precipitates. The reaction mixture is introduced into 320 parts of methanol, with stirring, and the mixture is stirred for 2 hours, without heating. The precipitated product is filtered off, washed with methanol and dried. 4.9 parts of ochre-coloured crude product which is purified by crystallisation from 50 parts of dimethylformamide, with addition of a filtration assistant, are obtained. 3.8 parts of 1,4-diketo-2,5-dibenzoyl-3,6-diphenylpyrrolo-[3,4-c]-pyrrole are obtained in the form of brownish-yellow crystals (formula XVIII). ##STR22##

後処理

  1. dissolutionThe starting material dissolves in the course of the reaction
  2. temperatureOn cooling of the reaction mixture, most of the reaction product
  3. customprecipitates
  4. additionThe reaction mixture is introduced into 320 parts of methanol
  5. stirringthe mixture is stirred for 2 hours
  6. temperaturewithout heating
  7. filtrationThe precipitated product is filtered off
  8. washwashed with methanol
  9. customdried
  10. filtration4.9 parts of ochre-coloured crude product which is purified by crystallisation from 50 parts of dimethylformamide, with addition of a filtration assistant
  11. customare obtained

出典と根拠

ORDレコード
ord-7b9b182c00dc45c498d95203e5af9e75
出典データセット
uspto-grants-1987_05
特許番号
US04666455

反応ノート

読み込み中…