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Dimethylformamide → 2,4-Difluoro-3-methylbenzaldehyde

HRID 1929604
ノート
印刷プレビュー

反応式

HRID 1929604 の反応式
[F:1][C:2]1[C:7]([CH3:8])=[C:6]([F:9])[CH:5]=[CH:4][C:3]=1Br.[Li]CCCC.CN([CH:19]=[O:20])C>C1COCC1>[F:1][C:2]1[C:7]([CH3:8])=[C:6]([F:9])[CH:5]=[CH:4][C:3]=1[CH:19]=[O:20]
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 112872263-Bromo-2,6-difluorotolueneHCID 178418339Butyllithium

生成物 1

HCID 121374892,4-Difluoro-3-methylbenzaldehyde

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

A cooled (−78° C.) solution of 2,4-difluoro-3-methylbromobenzene (2.000 g; 9.661 mmol) in anhydrous THF (36 ml) was treated dropwise (over 10 min.) with a solution of 1.6M n-BuLi in hexanes (6.04 ml; 9.661 mmol) while maintaining the temperature below −70° C. This mixture was further stirred at −78° C. for 2 min. before anhydrous DMF (1.49 ml; 19.326 mmol) was added dropwise (over 10 min.) while maintaining the temperature below −70° C. After completion of the addition, the resulting light brown solution was further stirred at −78° C. for 1 h30. The resulting mixture was then quenched at −78° C. with aq. sat. NH4Cl (10 ml), and was then allowed to warm-up to rt. Ether (50 ml) and water (20 ml) were added, and the organic layer was dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure (caution: rotary evaporation bath at 30° C. because the aldehyde is volatile). The crude was purified by FC (DCM) to give the pure product 2,4-difluoro-3-methyl-benzaldehyde as a pale yellow oil (1.250 g; 83%).

後処理

  1. temperaturewhile maintaining the temperature below −70° C
  2. additionwas added dropwise (over 10 min.)
  3. temperaturewhile maintaining the temperature below −70° C
  4. additionAfter completion of the addition
  5. customThe resulting mixture was then quenched at −78° C. with aq. sat. NH4Cl (10 ml)
  6. temperatureto warm-up to rt
  7. additionEther (50 ml) and water (20 ml) were added
  8. dry with materialthe organic layer was dried over anh. MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated to dryness under reduced pressure (caution
  11. customrotary evaporation bath at 30° C. because the aldehyde is volatile
  12. customThe crude was purified by FC (DCM)

出典と根拠

ORDレコード
ord-d6f79cf7fdbe4f20b6a3b85d4d3e20c6
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08188082B2

反応ノート

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