戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 37764作成日:2026年10月24日

3-(4-Hydroxyphenyl)propanol → 2-(4-Hydroxyphenyl)propanal

https://huagongshe.com/ja/reaction/37764

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4-Hydroxyphenyl)propanolHCID 82452—
反応物Sulfur trioxide-pyridineHCID 168533—
反応物4-HydroxyphenylacetaldehydeHCID 440113—
溶媒Dimethyl SulfoxideHCID 679—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Hydroxyphenyl)propanalHCID 1322718375%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524660B2
出典データセットuspto-grants-2013_09
ORD IDord-a7aacc3f8cea49a0a46cccab84016b4e
出典メモuspto-grants-2013_09