Chlorosuccinimide → 7-Acetyl-1,3-dihydro-2H-indol-2-one

HRID 1788965

反応式

HRID 1788965 の反応式
[C:1]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:12]=1[NH:11][CH:10]=[CH:9]2)(=[O:3])[CH3:2].ClN1C(=[O:19])CCC1=O>C(Cl)Cl>[C:1]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:12]=1[NH:11][C:10](=[O:19])[CH2:9]2)(=[O:3])[CH3:2]

参加物

4

反応物 2

HCID 31398ChlorosuccinimideHCID 137705341-(1H-indol-7-yl)ethanone

生成物 1

HCID 137705297-Acetyl-1,3-dihydro-2H-indol-2-one収率 65%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 12.57 g. (79 mmoles) of 7-acetylindole in 187 ml. of methylene chloride was added 11.07 g. (82.9 mmoles) of N-chlorosuccinimide and the reaction allowed to stir at room temperature for 2 hours. The solvent was removed in vacuo and the residue treated with 155 ml. of acetic acid and heated to 80° C. Phosphoric acid (80 ml.) was added and the reaction mixture heated to reflux for 9 hours. The mixture was cooled, the acetic acid removed under vacuum and the residue poured into 500 ml. of ice and water. The product was extracted with methylene chloride, 11.91 g. (65% yield), 174°-175° C.

後処理

  1. customThe solvent was removed in vacuo
  2. additionthe residue treated with 155 ml
  3. temperatureof acetic acid and heated to 80° C
  4. additionPhosphoric acid (80 ml.) was added
  5. temperaturethe reaction mixture heated
  6. temperatureto reflux for 9 hours
  7. temperatureThe mixture was cooled
  8. customthe acetic acid removed under vacuum
  9. additionthe residue poured into 500 ml
  10. extractionThe product was extracted with methylene chloride, 11.91 g
  11. custom(65% yield), 174°-175° C.

出典と根拠

ORDレコード
ord-ed0a6be47d0f43868578a84df4a040f4
出典データセット
uspto-grants-1987_08
特許番号
US04686224

関連ノート

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