반응 #66042

ord-a7aacc3f8cea49a0a46cccab84016b4e

반응 방정식

O=CCc1ccc(O)cc1
4-hydroxyphenylacetaldehyde
O=S(=O)=O.c1ccncc1
Pyridine-sulfur trioxide
OCCCc1ccc(O)cc1
3-(4-Hydroxyphenyl)-1-propanol
CC(C=O)c1ccc(O)cc1
4-hydroxyphenylpropionaldehyde
수율 75.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGAfter stirring for 1 h at room temperature
  2. 2
    세척washed with ice-cold water
  3. 3
    건조The organic layer was dried over Na2SO4
  4. 4
    여과filtered
  5. 5
    농축concentrated to dryness
  6. 6
    기타Purification

실험 절차

4-hydroxyphenylpropionaldehyde was prepared by a synthesis analogous to that for 4-hydroxyphenylacetaldehyde (Heterocycles, 2000, 53, 777-784). 3-(4-Hydroxyphenyl)-1-propanol (1.0 g, 6.6 mmol, Aldrich) was dissolved in dimethylsulfoxide (8 mL, Aldrich). TEA (2.0 mL, 14 mmol, Aldrich) was added slowly with stirring. Pyridine-sulfur trioxide (SO3.py) complex (2.3 g, 15 mmol, Aldrich) was completely dissolved in dimethylsulfoxide (9 mL, Aldrich) and this solution was added drop-wise to the alcohol, with vigorous stirring. After stirring for 1 h at room temperature, the reaction was diluted with CH2Cl2, then washed with ice-cold water. The organic layer was dried over Na2SO4, filtered, and concentrated to dryness. Purification using silica gel chromatography with hexane-ethyl acetate as eluent (5:1, then 2:1) yielded 745 mg (75%) of 4-hydroxyphenylpropionaldehyde.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08524660B2uspto-grants-2013_09