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HRID 28762作成日:2026年10月23日

Lead tetraacetate → p-Methoxyphenylpropionic acid

https://huagongshe.com/ja/reaction/28762

反応式

関与物質

役割名称HCID仕込み量
反応物Lead tetraacetateHCID 11025—
反応物Perchloric AcidHCID 24247—
反応物Ethyl orthoformateHCID 31214—
反応物4-PropanoylanisoleHCID 67144—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Potassium HydroxideHCID 14797—
生成物p-Methoxyphenylpropionic acidHCID 25757663.5%

反応条件

温度55 °C

反応手順

A mixture of p-methoxypropiophenone (2.39 g, 14.5 mmol), 90% lead(IV)acetate (6.45 g, 14.5 mmol), triethylorthoformate (15 ml) and 70% perchloric acid (1.2 ml. 29 mmol) was heated to 55° C. for 18 h. The mixture was cooled and the triethylorthoformate removed under reduced pressure. The residue was dissolved in CHCl3 and the remaining precipitate filtered off and discarded. The CHCl3 solution was then washed with water and evaporated to yield the crude ester. This crude ester product was dissolved in a 10% KOH 1:1 water:methanol solution, which was then refluxed for 3 h. After cooling the methanol was evaporated under reduced pressure and the aqueous solution washed with diethylether (3×25 ml). The aqueous solution was acidified with 2N H2SO4, then washed again with diethylether (3×25 ml). The combined fractions from the second ether wash were dried (Na2SO4) and evaporated to give the propionic acid (1.66 g, 63%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419998B2
出典データセットuspto-grants-2008_09
ORD IDord-296cb2a7bea74433a90a47142849b1ea
出典メモuspto-grants-2008_09