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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 373356생성일: 2026년 10월 24일

Ketoprofen → (S)-(-)-Ketoprofen cinchonidine

https://huagongshe.com/ko/reaction/373356

반응식

참여 물질

역할이름HCID투입량
반응물KetoprofenHCID 3825—
반응물Ethyl AcetateHCID 8857—
반응물CinchonidineHCID 101744—
용매MethanolHCID 887—
생성물(S)-(-)-Ketoprofen cinchonidineHCID 13171763931%

반응 조건

온도35 °C

반응 단계

Cinchonidine (155 g; 0.53 mol) was added to a solution of 115g (0.59 mol) of racemic ketoprofen and 2.8 L of ethyl acetate under vigorous stirring at 50°-60° C. The mixture was diluted with 280 mL of methanol, cooled to 35° C., then seeded with 98% enantiomerically pure S-salt to induce crystallization. After stirring at room temperature for 16 h and 0° C. for 5-6 h, the precipitated diastereomeric salt was filtered under vacuum, washed three times with ethyl acetate and three times with ether, and then dried under vacuum for 16 h [Yield: 127 g (or 44%); enantiomeric purity: 86% S]. One recrystallization from 1.7 L of ethyl acetate/methanol (10:1) afforded 88 g (31% yield) salt of 97% enantiomerically pure S-ketoprofen.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05162576
출처 데이터셋uspto-grants-1992_11
ORD IDord-59bbdc689ce24ee88b2bfe0a985a3868
출처 메모uspto-grants-1992_11