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Water → 3-(Bromomethyl)-2-fluorobenzonitrile

HRID 539311
ノート
印刷プレビュー

反応式

HRID 539311 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

HCID 666784653-(Bromomethyl)-2-fluorobenzonitrile収率 70.2%

試薬・触媒・溶媒 2

HCID 7187Benzoyl Peroxide触媒HCID 6342Acetonitrile溶媒

実験手順

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+.

後処理

  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

出典と根拠

ORDレコード
ord-09034a4e7e1e4757b50e413998ec2978
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08865911B2

反応ノート

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