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tert-Butyl methyl ether → 1-Chloro-3-fluoro-5-nitrobenzene

HRID 522799
ノート
印刷プレビュー

反応式

HRID 522799 の反応式
B1([O-])OO1.[OH2:5].[OH2:6].O.O.[Na+].[Cl:10][C:11]1[CH:12]=[C:13]([CH:15]=[C:16]([F:18])[CH:17]=1)[NH2:14].CC(OC)(C)C>C(O)(=O)C>[Cl:10][C:11]1[CH:12]=[C:13]([N+:14]([O-:6])=[O:5])[CH:15]=[C:16]([F:18])[CH:17]=1
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 15413tert-Butyl methyl etherHCID 27348383-Chloro-5-fluoroanilineHCID 23693097Sodium;3-oxidodioxaborirane;tetrahydrate

生成物 1

HCID 233688911-Chloro-3-fluoro-5-nitrobenzene収率 18.2%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

反応条件

温度
55 °C

実験手順

Sodium perborate tetrahydrate (7.69 g, 50.0 mmol) was suspended in 30 mL of acetic acid, and this suspension was warmed to 55° C. 3-Chloro-5-fluoroaniline (1.46 g, 10 mmol) was dissolved in 20 mL of acetic acid and added within one hour. The reaction was stirred for 1 hour at 55° C. and then cooled to room temperature. 300 mL of TBME was added, and the reaction mixture was filtered. The organic layer was washed with brine, followed by 20 mL of aqueous Na2S2O3, followed by brine. The organic layer was dried over Na2SO4 and concentrated under reduced pressure to give a residue, which was purified by column chromatography (40 g SiO2; cyclohexane) to yield the title compound as a solid (320 mg, 18%). 1H-NMR (400 MHz; DMSO-d6): 8.20 (s, 1H), 8.18 (d, 1H), 8.07 (d, 1H).

後処理

  1. additionadded within one hour
  2. temperaturecooled to room temperature
  3. filtrationthe reaction mixture was filtered
  4. washThe organic layer was washed with brine
  5. dry with materialThe organic layer was dried over Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. customto give a residue, which
  8. customwas purified by column chromatography (40 g SiO2; cyclohexane)

出典と根拠

ORDレコード
ord-2b5e73f8363b4225af4525025e69b8b4
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09334271B2

反応ノート

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