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Hydrogen Bromide → HCID 58572756、化合物

HRID 1927305
ノート
印刷プレビュー

反応式

HRID 1927305 の反応式
N[C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([F:10])=[CH:4][C:3]=1[C:11](=[O:13])[CH3:12].N([O-])=O.[Na+].[BrH:18]>[Cu](Br)Br>[Br:18][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([F:10])=[CH:4][C:3]=1[C:11](=[O:13])[CH3:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 260Hydrogen Bromide2 回HCID 23668193Sodium NitriteHCID 58572760HCID 58572760、化合物

生成物 1

HCID 58572756HCID 58572756、化合物収率 61%

試薬・触媒・溶媒 1

HCID 24611Copper bromide (CuBr2)触媒

反応条件

温度
0 °C

実験手順

1-(2-Amino-5-fluoro-3-methoxy phenyl)ethanone (2.66 g, 14.2 mmol), which had been obtained in Reference example 3(3b), was suspended in 10% aqueous hydrogen bromide solution (22 mL). Then, a 9% aqueous sodium nitrite solution (11 mL, 14.4 mmol) was slowly added dropwise thereto at 0° C. After stirring the mixture solution for 1 hour at 0° C., a solution in which copper bromide (I) (2.24 g, 15.7 mmol) is dissolved in 47% aqueous hydrogen bromide solution (15 mL) was added thereto, and the mixture was refluxed with heating at 110° C. for 2 hours. The reaction solution was cooled to room temperature and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (n-hexane/ethyl acetate=4/1) to give the title compound as a pale yellow solid (2.15 g, yield 61%).

後処理

  1. customat 0° C
  2. additionwas added
  3. temperaturethe mixture was refluxed
  4. temperaturewith heating at 110° C. for 2 hours
  5. temperatureThe reaction solution was cooled to room temperature
  6. extractionextracted with ethyl acetate
  7. washThe organic layer was washed with saturated brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. distillationThe solvent was distilled off under reduced pressure
  10. customThe residue was purified by silica gel chromatography (n-hexane/ethyl acetate=4/1)

出典と根拠

ORDレコード
ord-eb6b9a50dad34b45acc844173c270dfb
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08183272B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート