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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1395241생성일: 2026년 10월 26일

Ethanol → 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(phenylmethyl)piperazine maleate

https://huagongshe.com/reaction/1395241

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]piperazineHCID 9974013—
생성물1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(phenylmethyl)piperazine maleateHCID 70573504—

반응 단계

To a mixture of 6 g (0.018 mol) of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]piperazine (prepared as described in Example 3) and 3 g of potassium carbonate powder in 50 ml of ethanol, 3.1 g (0.018) of benzylbromide were added dropwise at room temperature. The reaction mixture was then slowly heated and refluxed for 3 hours. Subsequently another 3.1 g (0.018 mol) of benzylbromide were added dropwise at room temperature. The mixture was refluxed for 1.5 hours, cooled and filtered. The solvent was distilled off and the residue was purified by column chromatography (silicagel) with a mixture of chloroform and ethyl acetate (1:1) as the eluent. A solution of maleic acid in diethyl ether was added to the desired eluate fraction, the precipitate was filtered off and crystallized from a mixture of methanol and dimethylformamide. 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(phenylmethyl)piperazine maleate (1:2) was obtained. Melting point 201.5°-202.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04202896
출처 데이터셋uspto-grants-1980_05
ORD IDord-aa8b25ce4ef744a2a03b81f1b6eb3abe
출처 메모uspto-grants-1980_05