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HRID 231733생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/231733

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물3'-(Trifluoromethyl)acetophenoneHCID 67682—
반응물Ammonium AcetateHCID 517165—
반응물3,3-Bis(methylsulfanyl)-1-[4-(trifluoromethyl)phenyl]prop-2-EN-1-oneHCID 14551206—
반응물Potassium tert-butoxideHCID 23665647—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물4-(Methylthio)-2-(3-(trifluoromethyl)phenyl)-6-(4-(trifluoromethyl)phenyl)pyridineHCID 18941199.6%

반응 단계

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.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04849011
출처 데이터셋uspto-grants-1989_07
ORD IDord-aad2e82f5c7d4beaa8c357b3e6ebd071
출처 메모uspto-grants-1989_07