돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28762생성일: 2026년 10월 23일

Lead tetraacetate → p-Methoxyphenylpropionic acid

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

반응식

참여 물질

역할이름HCID투입량
반응물Lead tetraacetateHCID 11025—
반응물Perchloric AcidHCID 24247—
반응물Ethyl orthoformateHCID 31214—
반응물4-PropanoylanisoleHCID 67144—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Potassium HydroxideHCID 14797—
생성물p-Methoxyphenylpropionic acidHCID 25757663.5%

반응 조건

온도55 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419998B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-296cb2a7bea74433a90a47142849b1ea
출처 메모uspto-grants-2008_09