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Methyl iodide → 3-(2-Bromoethyl)-1-methyl-1H-indole

HRID 624051
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HRID 624051 반응식
[H-].[Na+].[CH3:3]I.[Br:5][CH2:6][CH2:7][C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[NH:10][CH:9]=1>C1COCC1>[Br:5][CH2:6][CH2:7][C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[N:10]([CH3:3])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 769243-(2-Bromoethyl)indole

생성물 1

HCID 131533063-(2-Bromoethyl)-1-methyl-1H-indole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A flask was charged with NaH (900 mg, 37.52 mmol), MeI (3.14 mL, 50.00 mmol) and THF (7.5 mL). The resulting grey suspension was stirred at rt for 5 min, then a solution of 3-(2-bromethyl)-indol (1.12 g, 5.00 mmol) in THF (25 mL) was added dropwise. After stirring for 18 h at rt, the reaction mixture was concentrated, redissolved in DCM and washed with H2O (3×). The org. layer was dried (MgSO4), filtered and the solvent was removed under reduced pressure to yield the title compound as an yellow oil which was used as such in the next step. LC-MS conditions A: tR=0.95 min, [M+H]+=no ionization.

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후처리

  1. stirringAfter stirring for 18 h at rt
  2. concentrationthe reaction mixture was concentrated
  3. dissolutionredissolved in DCM
  4. washwashed with H2O (3×)
  5. dry with materiallayer was dried (MgSO4)
  6. filtrationfiltered
  7. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-798d6f26c67040a19d0eab326fdd523e
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09303023B2

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