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Ethanol → Ethyl 6-chloro-1-methyl-1H-indole-2-carboxylate

HRID 1280397
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HRID 1280397 반응식
[H-].[Na+].[Cl:3][C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[NH:10]2)=[CH:6][CH:5]=1.IC.[CH2:20](O)C>CN(C)C=O>[Cl:3][C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[N:10]2[CH3:20])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 7015027Ethyl 6-chloroindole-2-carboxylate

생성물 1

HCID 10561874Ethyl 6-chloro-1-methyl-1H-indole-2-carboxylate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A suspension of 1.8 g (45 mmol) of 60% sodium hydride (washed beforehand with petroleum ether) and of 8.0 g (35.8 mmol) of ethyl 6-chloro-1H-indole-2-carboxylate in 80 ml of N,N-dimethylformamide is stirred for 2 h at room temperature, 2.8 ml (45 mmol) of iodomethane are subsequently added and the mixture is stirred at room temperature for 4 h. 5 ml of absolute ethanol are added and the solvent is evaporated under reduced pressure. The residue is taken up in water and the mixture is extracted with dichloromethane, the organic phase is dried and filtered, the solvent is evaporated under reduced pressure and the residue is purified by chromatography on a column of silica gel. 8.5 g (35.7 mmol) of a white crystalline compound are isolated.

후처리

  1. customthe solvent is evaporated under reduced pressure
  2. extractionthe mixture is extracted with dichloromethane
  3. customthe organic phase is dried
  4. filtrationfiltered
  5. customthe solvent is evaporated under reduced pressure
  6. customthe residue is purified by chromatography on a column of silica gel

출처 및 근거

ORD 기록
ord-74dd2f5c6d6c404b812efa3add7dc317
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06451795B1

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