戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 231733作成日:2026年10月26日

Sodium Hydroxide → 4-(Methylthio)-2-(3-(trifluoromethyl)phenyl)-6-(4-(trifluoromethyl)phenyl)pyridine

https://huagongshe.com/reaction/231733

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物3'-(Trifluoromethyl)acetophenoneHCID 67682—
反応物Ammonium AcetateHCID 517165—
反応物3,3-Bis(methylsulfanyl)-1-[4-(trifluoromethyl)phenyl]prop-2-EN-1-oneHCID 14551206—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
生成物4-(Methylthio)-2-(3-(trifluoromethyl)phenyl)-6-(4-(trifluoromethyl)phenyl)pyridineHCID 18941199.6%

反応手順

To 20 ml of tetrahydrofuran solution containing 0.64 g of m-trifluoromethylacetophenone was added 0.9 g of potassium t-butoxide at room temperature, followed by stirring for 30 minutes. Further, 1 g of 3,3-bis-(methylthio)-1-(4'-trifluoromethylphenyl)-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 portion 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 1.4 g of 2-(3'-trifluoromethylphenyl)-4-methylthio-6-(4'-trifluoromethylphenyl)pyridine. (m.p. 98.5° 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-aad2e82f5c7d4beaa8c357b3e6ebd071
出典メモuspto-grants-1989_07