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Methyl iodide → Methyl 5-methoxy-1-methyl-1H-indolecarboxylate

HRID 1459661
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HRID 1459661 반응식
[CH3:1]C(C)([O-])C.[K+].[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][C:13]([C:18]([O:20][CH3:21])=[O:19])=[CH:12]2.CI>O1CCCC1>[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14]([CH3:1])[C:13]([C:18]([O:20][CH3:21])=[O:19])=[CH:12]2
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 27281841H-Indole-2-carboxylic acid, 5-methoxy-, methyl esterHCID 23665647Potassium tert-butoxide

생성물 1

HCID 4777906Methyl 5-methoxy-1-methyl-1H-indolecarboxylate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매3회

실험 절차

100 ml of a 1N solution of potassium tert-butoxide in tetrahydrofuran is added dropwise to a solution, cooled to -20° C., of 0,1 mol of methyl 5-methoxy-1H-indolecarboxylate in tetrahydrofuran. The medium is stirred for 30 minutes at this temperature, followed by dropwise addition of a solution of 0.1 mol of methyl iodide in tetrahydrofuran. Once the addition is complete, the medium is warmed slowly to room temperature, stirred for 1 h at this temperature and filtered. The expected product is obtained after concentration of the solvent.

후처리

  1. additionOnce the addition
  2. stirringstirred for 1 h at this temperature
  3. filtrationfiltered

출처 및 근거

ORD 기록
ord-ddaf71314d9f4b8bac5118b05635acbe
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05854273

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