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Methyl iodide → 6-Bromo-2-methylbenzo[B]thiophene

HRID 226106
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HRID 226106 반응식
[CH:1](NC(C)C)(C)C.CN(CCN(C)C)C.[Li]CCCC.[Br:21][C:22]1[CH:23]=[CH:24][C:25]2[CH:29]=[CH:28][S:27][C:26]=2[CH:30]=1.CI>C1COCC1.C([O-])(O)=O.[Na+]>[Br:21][C:22]1[CH:23]=[CH:24][C:25]2[CH:29]=[C:28]([CH3:1])[S:27][C:26]=2[CH:30]=1
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참가 물질

8

반응물 5

HCID 6328Methyl iodideHCID 7912DiisopropylamineHCID 8037N,N,N',N'-TetramethylethylenediamineHCID 127444006-Bromo-benzo[b]thiopheneHCID 178418339Butyllithium

생성물 1

HCID 205951316-Bromo-2-methylbenzo[B]thiophene수율 95%

시약·촉매·용매 2

HCID 8028
Tetrahydrofuran
용매
2회
HCID 516892Sodium Bicarbonate용매

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온도
0 °C

실험 절차

Into a stirred solution of diisopropylamine (1.45 mL, 10.3 mmol) and TMEDA (3.4 mL, 22.5 mmol) in THF (30 mL, freshly distilled) at −78° C. is added 1.6 M n-BuLi (7.0 mL, 11.2 mmol) via a syringe. The solution is warmed to 0° C. for 30 min and re-cooled to −78° C. A solution of 6-bromobenzo[b]thiophene 2.0 g, 9.38 mmol) in THF (10 mL) is added via a cannula. After stirring for 30 min, a solution of CH3I (14.0 mL, 28.1 mmol, 2.0 M in tert-butyl methyl ether) is added via a cannula. The solution is stirred overnight, while allowed to warm to room temperature, and diluted with saturated aqueous NaHCO3 (50 mL). The mixture is extracted with Et2O (3×50 mL). The organic layers are combined, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a tan solid (2.0177 g, 95%).

후처리

  1. temperaturere-cooled to −78° C
  2. stirringThe solution is stirred overnight
  3. temperatureto warm to room temperature
  4. extractionThe mixture is extracted with Et2O (3×50 mL)
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-9325051da5144ad2926d2a2174af973f
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07557103B2

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