Nitric Acid → 1-Bromo-4-fluoro-2-methyl-5-nitrobenzene

HRID 522705

反応式

HRID 522705 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH3:9].[N+:10]([O-])([OH:12])=[O:11]>S(=O)(=O)(O)O>[Br:1][C:2]1[CH:7]=[C:6]([N+:10]([O-:12])=[O:11])[C:5]([F:8])=[CH:4][C:3]=1[CH3:9]

参加物

4

反応物 2

HCID 944Nitric AcidHCID 967432-Bromo-5-fluorotoluene

生成物 1

HCID 100369831-Bromo-4-fluoro-2-methyl-5-nitrobenzene収率 104.8%

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

Combine 1-bromo-4-fluoro-2-methylbenzene (30.0 g, 159 mmol) in concentrated sulfuric acid (100 mL), cool to about −5° C., and treat dropwise with nitric acid (11.00 mL, 174 mmol) over 20 minutes. Allow reaction mixture to warm to RT and stir for 30 min. Pour onto crushed ice with stirring and partition with tert-butyl methyl ether (MTBE) (200 mL). Separate the aqueous layer and extract with MTBE (2×50 mL). Combine organic layers, dry and concentrate under reduced pressure to provide 1-bromo-4-fluoro-2-methyl-5-nitrobenzene as an orange-colored viscous oil (39.0 g).

後処理

  1. customAllow reaction mixture
  2. additionPour
  3. customonto crushed ice
  4. stirringwith stirring
  5. custompartition with tert-butyl methyl ether (MTBE) (200 mL)
  6. customSeparate the aqueous layer
  7. extractionextract with MTBE (2×50 mL)
  8. customCombine organic layers, dry
  9. concentrationconcentrate under reduced pressure

出典と根拠

ORDレコード
ord-10aeb7632329498392241d80648555f9
出典データセット
uspto-grants-2016_05
特許番号
US09334267B2

関連ノート

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