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Chlorosuccinimide → 6-{[tert-Butyl(dimethyl)silyl]oxy}-3-chloro-1H-indole

HRID 1767978
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HRID 1767978 반응식
[Cl:1]N1C(=O)CCC1=O.[C:9]([Si:13]([CH3:25])([CH3:24])[O:14][C:15]1[CH:23]=[C:22]2[C:18]([CH:19]=[CH:20][NH:21]2)=[CH:17][CH:16]=1)([CH3:12])([CH3:11])[CH3:10]>ClCCl>[C:9]([Si:13]([CH3:25])([CH3:24])[O:14][C:15]1[CH:23]=[C:22]2[C:18]([C:19]([Cl:1])=[CH:20][NH:21]2)=[CH:17][CH:16]=1)([CH3:12])([CH3:11])[CH3:10]
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 222508166-((tert-butyldimethylsilyl)oxy)-1H-indole

생성물 1

HCID 236145106-{[tert-Butyl(dimethyl)silyl]oxy}-3-chloro-1H-indole수율 99%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of N-chlorosuccinimide (270 mg, 2 mmol) in dichloromethane (4 ml) is added within 30 min to a solution of 6-(tert-butyl-dimethyl-silanyloxy)-1H-indole (500 mg, 2 mmol) in dichloromethane (10 ml) at 0° C. under an argon atmosphere. The solution was naturally warmed to ambient temperature and stirred for 2 h. Ice water was added and the mixture was extracted two times with tert-butyl methyl ether. The combined extracts were dried over sodium sulfate and the solvent was removed under reduced pressure to give 560 mg (1.98 mmol, 98%) of the title compound as red solid which was used in the next step without further purification.

후처리

  1. extractionthe mixture was extracted two times with tert-butyl methyl ether
  2. dry with materialThe combined extracts were dried over sodium sulfate
  3. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-da882d7b0a95431a81a90d4471a06969
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07235572B2

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