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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1447701생성일: 2026년 10월 25일

Trifluoroacetic anhydride → [1-Oxo-2-(3-hydroxyphenyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid

https://huagongshe.com/reaction/1447701

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Lead monoxideHCID 14827—
반응물Ethyl(1-oxo-2-phenyl-2-methyl-6,7-dichloro-5-indanyloxy)acetateHCID 20384378—
용매Trifluoroacetic acidHCID 6422—
생성물[1-Oxo-2-(3-hydroxyphenyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acidHCID 2037823560%

반응 조건

온도25 °C

반응 단계

Ethyl(1-oxo-2-phenyl-2-methyl-6,7-dichloro-5-indanyloxy)acetate (18.95 g., 0.05 mole) dissolved in trifluoroacetic acid (100 ml.) is added portionwise at less than 10° C. to a stirred mixture of lead tetrakistrifluoroacetate (0.055 mole) prepared by stirring lead oxide (37.5 g.), trifluoroacetic acid (85 ml.) and trifluoroaceticanhydride (75 g.) at 25° C. for 96 hrs. After stirring the reaction mixture at 25° C. for 6 hours it is poured into crushed ice-water (1 l.) to precipitate 19.7 g. of a mixture of esters which is hydrolyzed by heating at reflux with ethanol (400 ml.) -water (250 ml.)-10 N sodium hydroxide solution (40 ml.) for 3/4 hr. On addition to crushed ice-water (1 l.)-12 N hydrochloric acid (50 ml.) a gummy product precipitates, is extracted with ether then concentrated to give 60% of [1-oxo-2-(3-hydroxyphenyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid and 20% of the 4-hydroxyphenyl derivative. Crystallization from acetic acid gives 2.6 g. of [1-oxo-2-(3-hydroxyphenyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid, m.p. 248°-255° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04177285
출처 데이터셋uspto-grants-1979_12
ORD IDord-5fcf14918425455ab8bd1821fb001ae8
출처 메모uspto-grants-1979_12