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p-Bromobenzenesulfonyl chloride → ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate

HRID 2264625
ノート
印刷プレビュー

反応式

HRID 2264625 の反応式
CC(C)([O-])C.[K+].C1OCCOCCOCCOCCOCCOC1.[NH:25]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[CH:27]=[C:26]1[C:34]([O:36][CH2:37][CH3:38])=[O:35].[Br:39][C:40]1[CH:45]=[CH:44][C:43]([S:46](Cl)(=[O:48])=[O:47])=[CH:42][CH:41]=1>C1COCC1.C(OCC)(=O)C>[Br:39][C:40]1[CH:45]=[CH:44][C:43]([S:46]([N:25]2[C:33]3[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=3)[CH:27]=[C:26]2[C:34]([O:36][CH2:37][CH3:38])=[O:35])(=[O:48])=[O:47])=[CH:42][CH:41]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 7396p-Bromobenzenesulfonyl chlorideHCID 2855718-Crown-6HCID 73125Ethyl indole-2-carboxylateHCID 23665647Potassium tert-butoxide

生成物 1

HCID 67043967ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate収率 95.3%

試薬・触媒・溶媒 2

HCID 8028
Tetrahydrofuran
溶媒
2 回
HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 0.5 g of potassium t-butoxide and 0.1 g of 18-crown-6 in 3 mL of THF, a mixed solution of 0.7 g of ethyl 1H-indole-2-carboxylate and 3 mL of THF was added, and the resulting mixture was stirred at room temperature for 30 minutes. The solution was cooled with ice, 1.13 g of 4-bromobenzenesulfonyl chloride was added, and the resulting mixture was stirred at room temperature for 5 hours. To the solution was added 60 mL of ethyl acetate, the resulting mixture was washed with water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:5) to obtain 1.44 g of ethyl 1-[(4-bromophenyl)sulfonyl]-1H-indole-2-carboxylate as a pale yellow syrup. FAB+: 408, 410

後処理

  1. additionwas added
  2. stirringthe resulting mixture was stirred at room temperature for 5 hours
  3. washthe resulting mixture was washed with water and saturated aqueous sodium chloride solution
  4. dry with materialdried over anhydrous sodium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:5)

出典と根拠

ORDレコード
ord-d6d5cf222d6e411eb1e67403140e4b05
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07855225B2

反応ノート

読み込み中…

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