反应 #66041

ord-52d55c87f4e34d32b565dac39979b5e0

反应方程式

O=S(=O)=O.c1ccncc1
Pyridine-sulfur trioxide
OCCc1ccc(O)cc1
4-Hydroxyphenethyl alcohol
O=CCc1ccc(O)cc1
4-hydroxyphenylacetaldehyde
收率 49.1%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他4-hydroxyphenylacetaldehyde (15) was synthesized
  2. 2
    workup.STIRRINGAfter stirring for 1 h at room temperature
  3. 3
    洗涤washed with ice-cold water
  4. 4
    干燥The organic layer was dried over Na2SO4
  5. 5
    过滤filtered
  6. 6
    浓缩concentrated to dryness
  7. 7
    其他Purification

实验过程

4-hydroxyphenylacetaldehyde (15) was synthesized as described in Heterocycles, 2000, 53, 777-784. 4-Hydroxyphenethyl alcohol (Compound 141.0 g, 7.3 mmol, Aldrich) was dissolved in dimethylsulfoxide (8 mL, Aldrich). With stirring, TEA (2.2 mL, 16 mmol, Aldrich) was added slowly. Pyridine-sulfur trioxide (SO3.py) complex (2.5 g, 16 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 488 mg (49%) of 4-hydroxyphenylacetaldehyde (15).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08524660B2uspto-grants-2013_09