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

HRID 522799
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HRID 522799 반응식
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
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참가 물질

5

반응물 3

HCID 15413tert-Butyl methyl etherHCID 27348383-Chloro-5-fluoroanilineHCID 23693097Sodium;3-oxidodioxaborirane;tetrahydrate

생성물 1

HCID 233688911-Chloro-3-fluoro-5-nitrobenzene수율 18.2%

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

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온도
55 °C

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-2b5e73f8363b4225af4525025e69b8b4
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09334271B2

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