2,4-Dihydroxybenzaldehyde → HCID 10537643、化合物

HRID 1955154ノート

反応式

HRID 1955154 の反応式
[OH:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[H-].[Na+].Cl[CH2:14][C:15]1[CH:19]=[CH:18][S:17][CH:16]=1>CN(C)C=O>[OH:1][C:2]1[CH:9]=[C:8]([O:10][CH2:14][C:15]2[CH:19]=[CH:18][S:17][CH:16]=2)[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5]

参加物

5

反応条件

温度
70 °C

実験手順

A stirred solution of 2,4-dihydroxybenzaldehyde (31.8 g) in dry dimethylformamide (150 ml) at ambient temperature was treated with sodium hydride (11.96 g; 60% dispersion in mineral oil), portionwise, during 30 minutes. After a further period of 15 minutes, the mixture was treated, dropwise, with a solution of 3-chloromethylthiophene (35 g) in dimethylformamide (50 ml). The mixture was stirred at 70° C. for 2 hours, cooled and the solvent evaporated. The residue was partitioned between ethyl acetate (200 ml) and 0.5 N hydrochloric acid (200 ml) and the aqueous layer was extracted twice with ethyl acetate (100 ml). The combined organic phases were washed with brine (100 ml), dried over magnesium sulphate, and evaporated. The residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and pentane (1:4, v/v), to give a colourless oil, which crystallised on standing. This solid was recrystallized from diisopropyl ether, to give the title compound (8 g) as a white solid.

後処理

  1. waitAfter a further period of 15 minutes
  2. additionthe mixture was treated
  3. temperaturecooled
  4. customthe solvent evaporated
  5. customThe residue was partitioned between ethyl acetate (200 ml) and 0.5 N hydrochloric acid (200 ml)
  6. extractionthe aqueous layer was extracted twice with ethyl acetate (100 ml)
  7. washThe combined organic phases were washed with brine (100 ml)
  8. dry with materialdried over magnesium sulphate
  9. customevaporated
  10. additionThe residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and pentane (1:4, v/v)
  11. customto give a colourless oil, which
  12. customcrystallised
  13. customThis solid was recrystallized from diisopropyl ether

出典と根拠

ORDレコード
ord-f0f6838ad0434665b59dbe3bdc29f8b9
出典データセット
uspto-grants-2000_09
特許番号
US06124343

反応ノート

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