Dimethylformamide → 2,4,6-Trichlorobenzaldehyde

HRID 246049

反応式

HRID 246049 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[CH:3]=1.[Li]CCCC.CN([CH:18]=[O:19])C>C1COCC1>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[CH:18]=[O:19]

参加物

5

反応条件

温度
-78 °C

実験手順

2,4,6-Trichlorobenzaldehyde was prepared according to the procedure outlined in Synthesis 2008, 279. To a solution of 1,3,5-trichlorobenzene (10.0 g, 55.1 mmol) in THF (200 ml) at −78° C. was slowly added n-BuLi (1.6 M in hexanes, 34.4 ml, 55.1 mmol) over 20 min. The reaction mixture was stirred at −78° C. for 30 min then DMF (7.5 ml, 96.4 mmol) was added dropwise. The reaction was stirred at −78° C. for an additional 1.5 h then quenched with 3 N HCl (200 ml) and warmed to room temperature. The mixture was extracted with EtOAc. The organic layer was washed with sat NaHCO3 and brine then dried over MgSO4 and concentrated to afford 10.7 g (93%) of 2,4,6-trichlorobenzaldehyde as a white solid.

後処理

  1. custom2,4,6-Trichlorobenzaldehyde was prepared
  2. customoutlined in Synthesis 2008, 279
  3. customat −78° C.
  4. customover 20 min
  5. stirringThe reaction was stirred at −78° C. for an additional 1.5 h
  6. customthen quenched with 3 N HCl (200 ml)
  7. temperaturewarmed to room temperature
  8. extractionThe mixture was extracted with EtOAc
  9. washThe organic layer was washed with sat NaHCO3 and brine
  10. dry with materialthen dried over MgSO4
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-8b87152df51643b3b7bba595d664ef10
出典データセット
uspto-grants-2014_02
特許番号
US08658646B2

関連ノート

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