Hydrochloric Acid → 3-Bromo-5-chlorobenzaldehyde

HRID 378166ノート

反応式

HRID 378166 の反応式
[Cl:1][C:2]1[CH:7]=[C:6](Br)[CH:5]=[C:4]([Br:9])[CH:3]=1.C([Li])CCC.CN([CH:18]=[O:19])C.Cl>C(OCC)C.CCCCCC>[Br:9][C:4]1[CH:5]=[C:6]([CH:7]=[C:2]([Cl:1])[CH:3]=1)[CH:18]=[O:19]

参加物

7

反応条件

温度
-30 °C

実験手順

To 1-chloro-3,5-dibromobenzene (Esprit) (20 g, 0.074 mole) in anhydrous ethyl ether (150 mL) in a flame dried flask under N2 and at -78° C. was added 1.6 m butyl lithium in hexane dropwise, keeping the temperature below -78° C., then warmed to -30° C. Anhydrous DMF (6.8 g, 0.092 mole) was added dropwise, keeping the temperature below -20° C. After the addition was complete, the reaction was slowly warmed to 0° C., then stirred overnight at room temperature. The reaction mixture was poured slowly into chilled 10% aqueous HCl (160 mL). After stirring for 15 minutes, the ether was separated, washed with H2O (4×), dried over MgSO4 and removed under vacuum to yield 3-bromo-5-chlorobenzaldehyde (13 g) as a white solid. MS and NMR were consistent with the desired structure.

後処理

  1. customthe temperature below -78° C.
  2. customthe temperature below -20° C
  3. additionAfter the addition
  4. temperaturethe reaction was slowly warmed to 0° C.
  5. additionThe reaction mixture was poured slowly
  6. stirringAfter stirring for 15 minutes
  7. customthe ether was separated
  8. washwashed with H2O (4×)
  9. dry with materialdried over MgSO4
  10. customremoved under vacuum

出典と根拠

ORDレコード
ord-3931a178d20c4e8a9886adb5e0e50830
出典データセット
uspto-grants-2000_02
特許番号
US06028223

反応ノート

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