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Sodium Iodide → 1-Bromo-4-(3-methoxypropoxy)benzene

HRID 1465564
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HRID 1465564 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[I-].[Na+].[C:11](=O)([O-])[O-].[K+].[K+].Cl[CH2:18][CH2:19][O:20][CH3:21]>C(#N)C.O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:11][CH2:18][CH2:19][O:20][CH3:21])=[CH:4][CH:3]=1
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참가 물질

7

반응물 4

HCID 5238Sodium IodideHCID 78084-BromophenolHCID 11430Potassium CarbonateHCID 123162-Chloroethyl methyl ether

생성물 1

HCID 219958541-Bromo-4-(3-methoxypropoxy)benzene수율 68%

시약·촉매·용매 2

HCID 962Water용매
HCID 6342
Acetonitrile
용매

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온도
60 °C

실험 절차

A mixture of 4-bromophenol (16-2, 1.01 g, 5.72 mmol), sodium iodide (1.02 g, 6.83 mmol), and potassium carbonate (1.88 g, 13.6 mmol) in acetonitrile (10.0 mL) was added with 1-chloro-2-methoxyethane (21-1, 0.89 g, 8.0 mmol). The mixture was heated to 60° C. for 48 h. The reaction mixture was cooled to room temperature and added with water (200 mL). The solution was extracted with EtOAc, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (EtOAc:hexanes=1:20 as eluant) to give 1-bromo-4-isopropoxybenzene (21-2, 0.95 g) as a colorless oil in 68% yield: 1H NMR (CDCl3) δ 7.36 (dt, J=5.0, 2.0 Hz, 2 H), 6.78 (m, 2 H), 4.02 (t, J=6.3 Hz, 2 H), 3.54 (t, J=6.1 Hz, 2 H), 3.35 (s, 3 H), 2.03 (t, J=6.2 Hz, 2 H).

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionThe solution was extracted with EtOAc
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by flash column chromatography on silica gel (EtOAc:hexanes=1:20 as eluant)

출처 및 근거

ORD 기록
ord-076b0e50185948219270ee2f8e49d426
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999983B2

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