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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37182생성일: 2026년 10월 23일

6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxin → 6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylmethyl}-1,4-benzodioxin

https://huagongshe.com/ko/reaction/37182

반응식

참여 물질

역할이름HCID투입량
반응물6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxinHCID 9804471—
반응물Aluminium lithium hydrideHCID 21226445—
용매Diethyl EtherHCID 3283—
생성물6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylmethyl}-1,4-benzodioxinHCID 1043389385%

반응 단계

Under a nitrogen atmosphere, heat at reflux for 3 hours, in the presence of 5 mmol of lithium aluminium hydride, a solution of 2 mmol of 6-hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxin in 35 cm3 of diethyl ether. After cooling, hydrolysis, removal of the insoluble mineral compounds by filtration and drying over magnesium sulfate, the compound obtained is purified by chromatography on a column of silica (eluant:petroleum ether/ethyl acetate, 40:60). 6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin -1-ylmethyl}-1,4-benzodioxin is thereby obtained in a yield of 85%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420132
출처 데이터셋uspto-grants-1995_05
ORD IDord-338a79a26a044e9f9f1fbe3ecf1e1c35
출처 메모uspto-grants-1995_05