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HRID 567191作成日:2026年10月25日

Hydrogen Peroxide → 2-[6-Fluoro-2-methyl-3-[(4-methylsulfonylphenyl)methylidene]inden-1-yl]acetic acid

https://huagongshe.com/reaction/567191

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物5-Fluoro-2-methyl-1-((4-(methylsulfinyl)phenyl)methylene)-1H-indene-3-acetic acidHCID 5352—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium MethoxideHCID 10942334—
反応物HCID 178418361HCID 178418361—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
生成物2-[6-Fluoro-2-methyl-3-[(4-methylsulfonylphenyl)methylidene]inden-1-yl]acetic acidHCID 11486689%

反応条件

温度0 °C

反応手順

5-Fluoro-2-methyl-1-(p-methylsulfonylbenzylidene)-3-indenyl acetic acid is prepared by adding sodium methoxide (4.4M in MeOH, 68.5 ml, 0.3 mol) dropwise to a stirred, cooled mixture of 5-fluoro-2-methyl-1-(p-methylsulfinylbenzylidene)-3-indenyl acetic acid (100 g, 0.281 mol) in methanol (250 ml) and acetonitrile (500 ml). Sodium bicarbonate (0.56 mol) and hydrogen peroxide (30% in water, 0.56 mol) are added and allowed to react for 18 hours at −10° C. Excess sodium bicarbonate is filtered off, and cooled filtrate (0° C.) neutralized dropwise to pH 7 with 1M hydrochloric acid (350 ml). The resulting product is then filtered and washed with methanol. A thin layer chromatography system to check for purity utilizes chloroform:methyl isobutyl ketone (8:2); the Rf value is 0.21. A tetrahydrofuran/diisopropyl ether combination can be used for product recrystallization. Reaction yield is 89%. (R1=5-fluoro; R2=CH3; R3=hydrogen; R4=COOH; R5=CH3SO2; n=1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06177471B1
出典データセットuspto-grants-2001_01
ORD IDord-3ff3e26b871e431db6ba2e01081c45b9
出典メモuspto-grants-2001_01