Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-carboxaldehyde

HRID 256391

反応式

HRID 256391 の反応式
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[CH2:3][CH2:2]1.ClC[CH:12]([O:15]C(CCl)CCl)CCl.C(=O)(O)[O-].[Na+]>C(Cl)Cl.[Ti](Cl)(Cl)(Cl)Cl>[CH:12]([C:8]1[CH:7]=[CH:6][C:5]2[O:1][CH2:2][CH2:3][C:4]=2[CH:9]=1)=[O:15]

参加物

6

実験手順

A solution of 9.4 ml (83.4 mmol) 2,3-dihydrobenzofuran in 250 ml methylene dichloride was cooled under nitrogen to 0° to -5° C. and 18 ml (167 mmole) titanium tetrachloride was added dropwise at 0° C. The resulting brown mixture was stirred 10 minutes and 8.3 ml (91.6 mmole) 1,1-dichloromethylmethyl ether was then added dropwise at 0° C. During this addition the reaction mixture became dark red in color. The mixture was allowed to warm to room temperature, stirred for 2 hours and poured slowly into a 2 liter beaker containing 700 ml saturated aqueous sodium bicarbonate solution The resulting mixture was filtered through diatomaceous earth and the solids washed with methylene dichloride. The separated organic layer was dried (Na2SO4) and the solvent evaporated to afford a residual oil, 10 g, (81%) which appeared homogeneous on silica gel thin-layer chromatography (TLC), eluting with an ethyl acetate/hexane/5% acetic acid, 1:5:5 by volume. Mass spectrum (m/e): 148 (M+), 147, 119.

後処理

  1. additionDuring this addition the reaction mixture
  2. stirringstirred for 2 hours
  3. additionpoured slowly into a 2 liter beaker
  4. filtrationwas filtered through diatomaceous earth
  5. washthe solids washed with methylene dichloride
  6. dry with materialThe separated organic layer was dried (Na2SO4)
  7. customthe solvent evaporated
  8. customto afford a residual oil, 10 g, (81%) which
  9. washeluting with an ethyl acetate/hexane/5% acetic acid, 1:5:5 by volume

出典と根拠

ORDレコード
ord-f0a401c2f49446cdb78279afe412c8a5
出典データセット
uspto-grants-1987_10
特許番号
US04703052

関連ノート

読み込み中…