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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263636생성일: 2026년 10월 26일

Ethanol → 5-Fluoro-2-methyl-1-((4-(methylsulfinyl)phenyl)methylene)-1H-indene-3-acetic acid

https://huagongshe.com/reaction/263636

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium HydroxideHCID 14798—
반응물N-[5-fluoro-2-methyl-1-(rho-methylsulfinylbenzylidene)-3-indenylacetyl]-glycineHCID 70150105—
용매WaterHCID 962—
생성물5-Fluoro-2-methyl-1-((4-(methylsulfinyl)phenyl)methylene)-1H-indene-3-acetic acidHCID 5352—

반응 단계

N-[5-fluoro-2-methyl-1-(ρ-methylsulfinylbenzylidene)-3-indenylacetyl]-glycine. Benzyle-N-[5-fluoro-2-methyl-1-(ρ-methylsulfinylbenzylidene)-3-indenylacetyl]-glycinate (0.03 mole) in a mixture of 25 ml. of anhydrous ethanol and 2.5 ml. of 1N sodium hydroxide is allowed to stand at room temperature for 18 hours. The solution is diluted with water and extracted with ether. The aqueous layer is acidified with dilute hydrochloric acid and the organic product is extracted with ethyl acetate, washed with water and dried over sodium sulfate. Evaporation of the solution gives N-[5-fluoro-2-methyl-1-(ρ-methylsulfinylbenzylidene)-3-indenylacetic acid, the corresponding indenyl acyl glycine is obtained, which can be converted to the corresponding sulfonyl derivative using the procedure of Example 1E.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05643959
출처 데이터셋uspto-grants-1997_07
ORD IDord-9f9891949e254cae9262f5b80d86bcca
출처 메모uspto-grants-1997_07