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

HRID 478899

反応式

HRID 478899 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
  3. waitfor three hours
  4. extractionextracted with ethyl acetate
  5. washThe combined extracts were washed with water several times
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customSilica gel chromatographic purification of the crude product

出典と根拠

ORDレコード
ord-dec07a13280d4c7ba505a26ef002596b
出典データセット
uspto-grants-2003_11
特許番号
US06642268B2

関連ノート

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