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HRID 231734作成日:2026年10月27日

Acetic Acid → 2-(3'-Chloromethylphenyl)-4-methylthio-6-phenylpyridine

https://huagongshe.com/reaction/231734

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium HydroxideHCID 14798—
反応物1-(3-Chlorophenyl)ethanoneHCID 14933—
反応物3,3-Bis(methylsulfanyl)-1-phenylprop-2-en-1-oneHCID 280923—
反応物Ammonium AcetateHCID 517165—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3'-Chloromethylphenyl)-4-methylthio-6-phenylpyridineHCID 20031588—

反応手順

To 20 ml of tetrahydrofuran solution containing 0.69 g of m-chloroacetophenone was added 1.1 g of potassium t-butoxide at room temperature, followed by stirring for 30 minutes. Further, 1 g of 3,3-bis-(methylthio)-1-phenyl-2-propen-1-one was added, followed by stirring for 1 hour. Subsequently, 20 ml of acetic acid and 3 g of ammonium acetate were added, and reaction was carried out for 3 hours under reflux, while distilling away tetrahydrofuran. The reaction liquid was neutralized with an aqueous solution of sodium hydroxide, and the neutralized solution was extracted twice with 50 ml portions of ethyl acetate. The extract was dried with anhydrous magnesium sulfate. Ethyl acetate was distilled away under reduced pressure and the residues were recrystallized from isopropanol to give 1.1 g of 2-(3'-chloromethylphenyl)-4-methylthio-6-phenylpyridine. (m.p. 56.8° C.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04849011
出典データセットuspto-grants-1989_07
ORD IDord-b0180c25d7db438096a5fdf4eb33bfd0
出典メモuspto-grants-1989_07