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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4751생성일: 2026년 10월 24일

Malonic Acid → 3-{2-Methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}-2-propenoic acid

https://huagongshe.com/ko/reaction/4751

반응식

참여 물질

역할이름HCID투입량
반응물Malonic AcidHCID 867—
반응물PiperidineHCID 8082—
반응물2-Methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzaldehydeHCID 14076652—
용매PyridineHCID 1049—
생성물3-{2-Methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}-2-propenoic acidHCID 5455527261%

반응 단계

To a solution of 15 g (0.05 mole) 2-methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzaldehyde in 50 ml of pyridine are added 11 g (0.11 mole) of malonic acid and 1 g of piperidine. The solution is stirred and gradually heated to 80°. Heating and stirring are continued for 1 hour at 80°. The solution is then heated at reflux for an additional 3 hours, cooled, and evaporated at reduced pressure to obtain a residual oil which is extracted into ether. The resulting ether solution is washed with water and 1N hydrochloric acid, dried with anhydrous magnesium sulfate, filtered, and evaporated at reduced pressure to obtain a residual solid which is recrystallized from chlorobutane/hexane mixed solvent to give 10.5 g of 3-{2 -methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}-2-propenoic acid having a melting point of 138°-140°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727180
출처 데이터셋uspto-grants-1988_02
ORD IDord-ec0779edb24c45fe9d209facc9386718
출처 메모uspto-grants-1988_02