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Dimethylformamide → 1,2-Dimethyl-1H-indole-3-carboxaldehyde

HRID 225901
ノート
印刷プレビュー

反応式

HRID 225901 の反応式
O=P(Cl)(Cl)Cl.[CH3:6][N:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[C:8]1[CH3:16].[OH-].[Na+].CN([CH:22]=[O:23])C>O>[CH3:6][N:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:9]([CH:22]=[O:23])=[C:8]1[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6228DimethylformamideHCID 134081,2-DimethylindoleHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychloride

生成物 1

HCID 5990841,2-Dimethyl-1H-indole-3-carboxaldehyde収率 97%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

このページの内容参加物実験手順後処理出典と根拠反応ノート

A solution of POCl3 (7.0 mL, 75 mmole) in DMF (100 mL) was stirred for 5 minutes at 0° C., then 1,2-dimethylindole (10.0 g, 69 mmole) was added in one portion. The reaction was allowed to warm to RT and stirred for 4 h. The thick slurry was poured into ice water (300 mL) and the flask was rinsed with additional water (50 mL). The aqueous mixture was basified with a solution of NaOH (13.2 g, 330 mmole) in H2O (50 mL), and the thick suspension was filtered to collect the solid. This was washed with water and dried under vacuum to give the title compound (11.59 g, 97%) as an off-white solid:

後処理

  1. washthe flask was rinsed with additional water (50 mL)
  2. filtrationthe thick suspension was filtered
  3. customto collect the solid
  4. washThis was washed with water
  5. customdried under vacuum

出典と根拠

ORDレコード
ord-4b1b7dedbeee41f8baa394c3b77c2a98
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07557125B2

反応ノート

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