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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 441403생성일: 2026년 10월 26일

Potassium Iodide → 1-[gamma-(2-Methyl-4-fluorobenzoyl)-propyl]-4-(3-trifluoromethylphenyl)-4-hydroxypiperidine

https://huagongshe.com/reaction/441403

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물4-[3-(Trifluoromethyl)phenyl]-4-piperidinolHCID 75255—
반응물2-(3-Chloropropyl)-2-(4-fluoro-2-methylphenyl)-1,3-dioxolaneHCID 13002954—
용매DimethylformamideHCID 6228—
생성물1-[gamma-(2-Methyl-4-fluorobenzoyl)-propyl]-4-(3-trifluoromethylphenyl)-4-hydroxypiperidineHCID 13002955—

반응 단계

A mixture of 3 g of 4-chloro-1-(2-methyl-4-fluorophenyl)-1,1-ethylenedioxybutane, 2.5 g of 4-(3-trifluoromethylphenyl)-4-hydroxypiperidine, 1,4 g of anhydrous potassium carbonate, 0.05 g of potassium iodide and 30 ml of dimethylformamide was refluxed for 3 hours. The resulting mixture was poured into ice water and was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and concentrated in vacuo. To the residual oil were added 60 ml of methanol, 21 ml of water and 10.5 ml of concentrated hydrochloric acid. The mixture was refluxed for 50 minutes and concentrated in vacuo. The residual oil was made alkaline with 28 % aqueous ammonia and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and concentrated. The residual solid was recrystallized from isopropyl ether to give 1-[γ-(2-methyl-4-flourobenzoyl)-propyl]-4-(3-trifluoromethylphenyl)-4-hydroxypiperidine, melting at about 63.5°-64.5+ C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04039670
출처 데이터셋uspto-grants-1977_08
ORD IDord-927041b00c9243889702d8e1c647dfc7
출처 메모uspto-grants-1977_08