Nitric Acid → 2-[2-(4-Bromo-2-nitrophenyl)propyl]pyridine

HRID 1579373ノート

反応式

HRID 1579373 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:16])[CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=2)=[CH:4][CH:3]=1.[N+:17]([O-])([OH:19])=[O:18]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:16])[CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=2)=[C:4]([N+:17]([O-:19])=[O:18])[CH:3]=1

参加物

3

反応物 2

HCID 944Nitric AcidHCID 205600682-[2-(4-Bromophenyl)propyl]pyridine

生成物 1

HCID 205599842-[2-(4-Bromo-2-nitrophenyl)propyl]pyridine

実験手順

2-(p-Bromophenyl)-1-(2-pyridyl)propane (11.5 g., 0.043 mole) is heated in 80 ml. of concentrated nitric acid (specific gravity 1.42, 69-71%) for 4.5 hr. at 80°C. The solution is cooled, quenched in 300 g. of ice, made alkaline with sodium hydroxide, and extracted with ethyl acetate. The extract washed with water and brine, dried over sodium sulfate, and evaporated affords 12.2 g. (88%) of oily nitrated product of sufficient purity to be used in following "step d". Distillation provides analytically pure 2-(4-bromo-2-nitrophenyl)-1-(2-pyridyl)propane, b.p. 172°-176°C. (0.2 mm. Hg.), nD 29 1.5968.

後処理

  1. customat 80°C
  2. temperatureThe solution is cooled
  3. customquenched in 300 g
  4. extractionextracted with ethyl acetate
  5. washThe extract washed with water and brine
  6. dry with materialdried over sodium sulfate
  7. customevaporated
  8. customaffords 12.2 g
  9. distillationDistillation

出典と根拠

ORDレコード
ord-1a8517b4380147248f070ec961b5d6a1
出典データセット
uspto-grants-1976_01
特許番号
US03931195

反応ノート

読み込み中…