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Iodoethane → 7-Bromo-1-ethyl-1H-indole

HRID 2215757
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인쇄 미리보기

반응식

HRID 2215757 반응식
[H-].[Na+].[Br:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:12]=1[NH:11][CH:10]=[CH:9]2.I[CH2:14][CH3:15]>CN(C=O)C>[CH2:14]([N:11]1[C:12]2[C:8](=[CH:7][CH:6]=[CH:5][C:4]=2[Br:3])[CH:9]=[CH:10]1)[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 24758Sodium hydrideHCID 27570207-Bromoindole

생성물 1

HCID 219500327-Bromo-1-ethyl-1H-indole

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

To a 60% dispersion of sodium hydride in mineral oil (0.80 g, 21 mmol), suspended in DMF (50 mL), was added 7-bromoindole (2.0 g, 10 mmol) in DMF (15 mL) followed by a solution of iodoethane (1.64 mL, 26.3 mmol). After 20 minutes, the mixture was quenched with saturated NaHCO3, and poured into EtOAc. The organic layer which was separated, washed with saturated NaHCO3, dried (MgSO4) and concentrated to afford 1-ethyl-7-bromoindole as a brown oil which was used without further purification.

후처리

  1. customthe mixture was quenched with saturated NaHCO3
  2. additionpoured into EtOAc
  3. customThe organic layer which was separated
  4. washwashed with saturated NaHCO3
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9712799578c0460bbdfc717df6861f72
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07109229B2

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