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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1460224생성일: 2026년 10월 27일

Potassium Iodide → 4-[3-[4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxybenzoic acid methyl ester

https://huagongshe.com/reaction/1460224

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium CarbonateHCID 10340—
반응물Bis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
반응물Methyl 4-(3-chloropropoxy)-3-methoxybenzoateHCID 14407173—
용매DimethylformamideHCID 6228—
생성물4-[3-[4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidinyl]propoxy]-3-methoxybenzoic acid methyl esterHCID 14407129—

반응 단계

A mixture of α,α-bis(4-fluorophenyl)-4-piperidinemethanol (6.0 g, 0.02 mole), 4-(3-chloropropoxy)-3-methoxybenzoic acid methyl ester (5.4 g, 0.021 mole), anhydrous sodium carbonate (7.4 g, 0.07 mole), and potassium iodide (0.3 g) in 150 ml of dimethylformamide was heated on a steam bath for about 20 hr. The mixture was concentrated under reduced pressure, and the residue was partitioned between water and organic solvent (benzene). The organic layer was washed with water and brine and dried over sodium sulfate and eventually crystallized from 2-propanol to give the title compound as a white solid, mp 131°-132.5° C. (2-propanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05070087
출처 데이터셋uspto-grants-1991_12
ORD IDord-d8c712e2c274493f9acf7df88534363b
출처 메모uspto-grants-1991_12