Dimethyl Sulfoxide → 3-Fluorobenzene-1,2-dicarbaldehyde

HRID 496179

反応式

HRID 496179 の反応式
[F:1][C:2]1[CH:9]=[CH:8][C:7](F)=[CH:6][C:3]=1[CH:4]=[O:5].[S-2].[Li+].[Li+].[OH2:14].[CH3:15]S(C)=O>>[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:15]=[O:14])[C:3]=1[CH:4]=[O:5]

参加物

5

実験手順

To a stirred solution of 17.5 g (123 mmol) of 2,5-difluorobenzaldehyde (Aldrich) in 615 mL of DMSO at ambient temperature was added 6.2 g (135 mmol) of lithium sulfide (Aldrich). The dark red solution was stirred at 75 C for 1.5 hours, or until the starting material was completely consumed, and then 34 g (135 mmol) of dibutyl mesylate aldehyde was added at about 50 C. The reaction mixture was stirred at 75 C for three hours or until the reaction was completed. The cooled solution was poured into water and extracted with ethyl acetate. The combined extracts were washed with water several times, dried (MgSO4) and concentrated in vacuo. Silica gel chromatographic purification of the crude product gave 23.6 g (59%) of fluorobenzene dialdehyde as a yellow oil: 1H NMR (CDCl3) d 0.87 (t, J=7.05 Hz, 6H), 1.0-1.4 (m, 8H), 1.5-1.78 (m, 4H), 3.09 (s, 2H), 7.2-7.35 (m, 1H), 7.5-7.6 (m, 2H), 9.43 (s, 1H) 10.50 (d, J=2.62 Hz, 1H)

後処理

  1. customuntil the starting material was completely consumed
  2. stirringThe reaction mixture was stirred at 75 C for three hours or until the reaction
  3. extractionextracted with ethyl acetate
  4. washThe combined extracts were washed with water several times
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customSilica gel chromatographic purification of the crude product

出典と根拠

ORDレコード
ord-19c0894312d14027be594246d09d1d8d
出典データセット
uspto-grants-2005_09
特許番号
US06943189B2

関連ノート

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