Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-carboxaldehyde

HRID 256391

반응식

HRID 256391 반응식
[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]

참가 물질

6

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f0a401c2f49446cdb78279afe412c8a5
출처 데이터셋
uspto-grants-1987_10
특허 번호
US04703052

연결된 노트

불러오는 중…