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Water → 3-(Bromomethyl)-2-fluorobenzonitrile

HRID 539311
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HRID 539311 반응식
C1C(=O)N([Br:8])C(=O)C1.[F:9][C:10]1[C:17]([CH3:18])=[CH:16][CH:15]=[CH:14][C:11]=1[C:12]#[N:13].O>C(#N)C.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>[Br:8][CH2:18][C:17]1[C:10]([F:9])=[C:11]([CH:14]=[CH:15][CH:16]=1)[C:12]#[N:13]
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참가 물질

6

반응물 3

HCID 962WaterHCID 67184N-bromobutanimideHCID 231603592-Fluoro-3-methylbenzonitrile

생성물 1

HCID 666784653-(Bromomethyl)-2-fluorobenzonitrile수율 70.2%

시약·촉매·용매 2

HCID 7187Benzoyl Peroxide촉매HCID 6342Acetonitrile용매

실험 절차

NBS (1.729 g, 9.71 mmol) was added to a solution of 2-fluoro-3-methylbenzonitrile (1.25 g, 9.25 mmol) in acetonitrile (25 mL). The obtained mixture was refluxed, and then benzoic peroxyanhydride (0.045 g, 0.18 mmol) was added. The reaction mixture was refluxed overnight, then cooled to r.t. and water was added. The aqueous phase was discarded and the organic phase was dried over MgSO4 and concentrated. The crude product was purified by flash chromatography using a gradient of EtOAc in heptane as eluent to give the title compound (1.39 g, 70% yield): 1H NMR (500 MHz, DMSO-d6) δ ppm 4.75 (s, 2 H) 7.43 (t, 1 H) 7.93 (t, 2 H); MS (EI) m/z 213 M+.

후처리

  1. temperatureThe obtained mixture was refluxed
  2. temperatureThe reaction mixture was refluxed overnight
  3. dry with materialthe organic phase was dried over MgSO4
  4. concentrationconcentrated
  5. customThe crude product was purified by flash chromatography

출처 및 근거

ORD 기록
ord-09034a4e7e1e4757b50e413998ec2978
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08865911B2

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