Nitric Acid → 5'-Fluoro-2'-hydroxy-3'-nitroacetophenone

HRID 325744

反応式

HRID 325744 の反応式
[CH3:1][C:2]([C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:5]=1[OH:11])=[O:3].[N+:12]([O-])([OH:14])=[O:13].O>S(=O)(=O)(O)O>[CH3:1][C:2]([C:4]1[C:5]([OH:11])=[C:6]([N+:12]([O-:14])=[O:13])[CH:7]=[C:8]([F:10])[CH:9]=1)=[O:3]

参加物

5

反応物 3

HCID 944Nitric AcidHCID 962WaterHCID 959922-Acetyl-4-fluorophenol

生成物 1

HCID 27589845'-Fluoro-2'-hydroxy-3'-nitroacetophenone

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒2 回

反応条件

温度
-20 °C

実験手順

5-Fluoro-2-hydroxyacetophenone (20.0 g) was dissolved in concentrated sulphuric acid (150 ml), and the mixture was cooled to -20° C. A mixture of concentrated nitric acid (17.0 ml; s.g. 1.42) in concentrated sulphuric acid (18.0 ml) was then added to it, dropwise with stirring, keeping the temperature of the reaction mixture between -15° and -5° C. The reaction mixture was then allowed to warm up to -5° C. and was poured into iced water (2 liters). The yellow precipitated product was filtered off and recrystallised from ethanol to give 5-fluoro-2-hydroxy-3-nitroacetophenone (11.9 g), m.p. 87°-90° C.

後処理

  1. additionwas then added to it
  2. customthe temperature of the reaction mixture between -15° and -5° C
  3. temperatureto warm up to -5° C.
  4. filtrationThe yellow precipitated product was filtered off
  5. customrecrystallised from ethanol

出典と根拠

ORDレコード
ord-1cbee42d0ddd47a0969e630c7e489cba
出典データセット
uspto-grants-1984_04
特許番号
US04442115

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