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Water → 1-(2-Bromoethoxy)-2-nitrobenzene

HRID 1498150
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HRID 1498150 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])([O-:3])=[O:2].[OH-].[Na+].O.[Br:14][CH2:15][CH2:16]Br>>[Br:14][CH2:15][CH2:16][O:10][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[N+:1]([O-:3])=[O:2]
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참가 물질

5

반응물 4

HCID 962WaterHCID 69472-NitrophenolHCID 78391,2-DibromoethaneHCID 14798Sodium Hydroxide

생성물 1

HCID 3100071-(2-Bromoethoxy)-2-nitrobenzene수율 63%

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온도
107 °C

실험 절차

To 2-nitrophenol (25.0 g, 0.180 mol) in sodium hydroxide (14.4 g, 359 mmol) and Water (6.0 mL, 330 mmol) in a 500 mL flask at 107° C. with a reflux condenser was added 1,2-dibromoethane (61.9 mL, 719 mmol), and the flask was heated at 107° C. for three days (FIG. 18). Then, the product was extracted twice with 100 mL DCM, washed with 2M NaOH and brine, dried with sodium sulfate, and concentrated. Silica gel chromatography eluting with hexanes and ethyl acetate provided the bromide 82 in 63% yield. 1H NMR (500 MHz, CDCl3) δ 7.83 (dd, J=8.4, 1.6 Hz, 1H), 7.53 (td, J=8.1, 1.6 Hz, 1H), 7.12-7.01 (m, 2H), 4.45-4.34 (m, 2H), 3.67 (t, J=6.5 Hz, 2H), according to: WO 2002076926

후처리

  1. extractionThen, the product was extracted twice with 100 mL DCM
  2. washwashed with 2M NaOH and brine
  3. dry with materialdried with sodium sulfate
  4. concentrationconcentrated
  5. washSilica gel chromatography eluting with hexanes and ethyl acetate

출처 및 근거

ORD 기록
ord-4d343f9457ff41d8b322ad646180a346
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09198918B2

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