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Dimethylformamide → 2,4,6-Trichlorobenzaldehyde

HRID 246049
ノート
印刷プレビュー

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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 79501,3,5-TrichlorobenzeneHCID 178418339Butyllithium

生成物 1

HCID 53144572,4,6-Trichlorobenzaldehyde収率 93%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

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
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658646B2

反応ノート

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