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

HRID 2264625
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인쇄 미리보기

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HRID 2264625 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

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

생성물 1

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

시약·촉매·용매 2

HCID 8028
Tetrahydrofuran
용매
2회
HCID 8857Ethyl Acetate용매

실험 절차

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

후처리

  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)

출처 및 근거

ORD 기록
ord-d6d5cf222d6e411eb1e67403140e4b05
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07855225B2

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