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N-Iodosuccinimide → 5-Iodoindolin-2-one

HRID 24351
ノート
印刷プレビュー

反応式

HRID 24351 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[I:11]N1C(=O)CCC1=O>C(O)(=O)C>[I:11][C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][C:2](=[O:10])[CH2:3]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 120273N-IodosuccinimideHCID 321710Oxindole

生成物 1

HCID 98380455-Iodoindolin-2-one収率 58%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
10 °C

実験手順

2-Oxindole (82.9 g) was suspended in 630 ml of acetic acid in a reaction vessel equipped with mechanical stirring and the mixture cooled to 10° C. in an ice water bath. Solid N-iodosuccinimide (175 g) was added in portions over 10 minutes. After the addition was complete the mixture was stirred for 1 hour at 10° C. The suspended solid which was always present became very thick at this time. The solid was collected by vacuum filtration, washed with 100 ml of 50% acetic acid in water and then with 200 ml of water and subjected to vacuum filtration for 20 minutes to partially air dry it. The product was then dried under vacuum to give 93.5 g (36%) of 5-iodo-2-oxindole containing about 5% 2-oxindole by proton NMR.

後処理

  1. customequipped
  2. additionAfter the addition
  3. stirringwas stirred for 1 hour at 10° C
  4. filtrationThe solid was collected by vacuum filtration
  5. washwashed with 100 ml of 50% acetic acid in water
  6. filtrationwith 200 ml of water and subjected to vacuum filtration for 20 minutes
  7. customto partially air dry it
  8. customThe product was then dried under vacuum

出典と根拠

ORDレコード
ord-4a7946c73d2e4a1ea6fd09f45d66fa9d
出典データセット
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06855730B2

反応ノート

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