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Carbon Dioxide → 1,4-dimethyl-1H-indole-2-carboxylic acid

HRID 1761068
ノート
印刷プレビュー

反応式

HRID 1761068 の反応式
[CH3:1][N:2]1[C:10]2[C:5](=[C:6]([CH3:11])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3]1.[Li]CCCC.[C:17](=[O:19])=[O:18].O>CCOCC>[CH3:1][N:2]1[C:10]2[C:5](=[C:6]([CH3:11])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]1[C:17]([OH:19])=[O:18]
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 280Carbon DioxideHCID 962WaterHCID 5893891,4-DimethylindoleHCID 178418339Butyllithium

生成物 1

HCID 47777991,4-dimethyl-1H-indole-2-carboxylic acid収率 26.4%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

A solution of 1,4-dimethyl-1H-indole (0.9 g, 6.2 mmole) in anhydrous Et2O (20 mL) was treated with 2.5 M n-BuLi in hexanes (5.0 mL, 12 mmole) and the reaction was heated at reflux for 15 hr. The dark reaction mixture was poured into a slurry of excess crushed dry ice in Et2O, and the mixture was allowed to stand for 1 hr. Water (10 mL) was added, the layers separated, and the aqueous layer was filtered through celite®P. The clear filtrate was acidified with 2.0 N HCl to pH 2, and the precipitate was collected and dried to afford the title compound (0.29 g, 26.4%) as an off-white solid: MS (ES) m/e 190.2 (M+H)+.

後処理

  1. temperaturethe reaction was heated
  2. temperatureat reflux for 15 hr
  3. customThe dark reaction mixture
  4. additionwas poured into a slurry
  5. customthe layers separated
  6. filtrationthe aqueous layer was filtered through celite®P
  7. customthe precipitate was collected
  8. customdried

出典と根拠

ORDレコード
ord-1f8d5b6455714a3984640b11a2b5ed24
出典データセット
uspto-grants-2005_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06846819B1

反応ノート

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