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Potassium Nitrate → 1-Bromo-5-fluoro-2-methyl-4-nitrobenzene

HRID 536340
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HRID 536340 반응식
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH3:9].[N+:10]([O-])([O-:12])=[O:11].[K+]>S(=O)(=O)(O)O.O>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([N+:10]([O-:12])=[O:11])=[CH:4][C:3]=1[CH3:9]
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참가 물질

5

반응물 2

HCID 24434Potassium NitrateHCID 740162-Bromo-4-fluorotoluene

생성물 1

HCID 534032861-Bromo-5-fluoro-2-methyl-4-nitrobenzene

시약·촉매·용매 2

HCID 962Water용매HCID 1118Sulfuric Acid용매2회

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온도
0 °C

실험 절차

To a solution of 2-bromo-4-fluoro-1-methylbenzene (5 g, 26.4 mmol) dissolved in conc. sulfuric acid (20 mL) was added potassium nitrate (2.67 g, 26.4 mmol) in sulfuric acid (5 mL) at 0° C. After stirring at 0° C. for 1 hr, the reaction was diluted with water, extracted with ethyl acetate (3×40 mL). The combined organic phases were washed with saturated sodium bicarbonate solution and brine sequentially, and then dried over Na2SO4. The crude product obtained after concentration was purified by silica gel column chromatography with mixed solvent hexanes/EtOAc (95/5) to afford 1-bromo-5-fluoro-2-methyl-4-nitrobenzene as an orange solid. 1H NMR (400 MHz, chloroform-d) δ 7.93 (d, 1H, J=7.6 Hz), 7.50 (d, 1H, J=10 Hz), 2.43 (s, 3H).

후처리

  1. extractionextracted with ethyl acetate (3×40 mL)
  2. washThe combined organic phases were washed with saturated sodium bicarbonate solution and brine sequentially
  3. dry with materialdried over Na2SO4
  4. customThe crude product obtained
  5. concentrationafter concentration
  6. customwas purified by silica gel column chromatography with mixed solvent hexanes/EtOAc (95/5)

출처 및 근거

ORD 기록
ord-85ffd01ab0b7416b920413f70b2db7cb
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859574B2

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