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Nitric Acid → 1,3-Dibromo-5-fluoro-2-methoxy-4-nitrobenzene

HRID 33405
ノート
印刷プレビュー

反応式

HRID 33405 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4]([Br:9])[C:3]=1[O:10][CH3:11].[N+:12]([O-])([OH:14])=[O:13]>OS(O)(=O)=O>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([N+:12]([O-:14])=[O:13])=[C:4]([Br:9])[C:3]=1[O:10][CH3:11]
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

4

反応物 2

HCID 944Nitric AcidHCID 27739651,3-Dibromo-5-fluoro-2-methoxybenzene

生成物 1

HCID 225046691,3-Dibromo-5-fluoro-2-methoxy-4-nitrobenzene収率 95%

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒2 回

反応条件

温度
4 °C

実験手順

To a stirred solution of c.H2SO4 (740 mL) at 0 to 5° C. was added 1,3-dibromo-5-fluoro-2-methoxybenzene (223.3 g, 0.786 mol). A solution of fuming nitric acid (90%, 38 mL, 0.815 mol) in c.H2SO4 (740 mL) was added dropwise, maintaining the temperature between 0 and 5° C. The reaction mixture was stirred at 3 to 5° C. for 2 hours, quenched into ice (2.2 kg) and extracted with dichloromethane (3×2 L). The combined dichloromethane extracts were washed with saturated aqueous NaHCO3 solution (2×2 L), dried over Na2SO4, filtered and the filter cake washed with DCM (3×400 mL). The filtrate was concentrated in vacuo at 40° C. to give 1,3-Dibromo-5-fluoro-2-methoxy-4-nitrobenzene as a pale orange crystalline solid (244.9 g, 95%).

後処理

  1. temperaturemaintaining the temperature between 0 and 5° C
  2. customquenched into ice (2.2 kg)
  3. extractionextracted with dichloromethane (3×2 L)
  4. washThe combined dichloromethane extracts were washed with saturated aqueous NaHCO3 solution (2×2 L)
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. washthe filter cake washed with DCM (3×400 mL)
  8. concentrationThe filtrate was concentrated in vacuo at 40° C.

出典と根拠

ORDレコード
ord-417708790e7142aea303520839496f61
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07429598B2

反応ノート

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