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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227293생성일: 2026년 10월 24일

((Chloromethyl)sulphonyl)benzene → 1-Benzyl-4-{4-nitro-3-[(phenylsulfonyl)methyl]phenyl}piperazine

https://huagongshe.com/ko/reaction/227293

반응식

참여 물질

역할이름HCID투입량
반응물((Chloromethyl)sulphonyl)benzeneHCID 81625—
반응물1-Benzyl-4-(4-nitrophenyl)piperazineHCID 2747427—
반응물HCID 178418922HCID 178418922—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-4-{4-nitro-3-[(phenylsulfonyl)methyl]phenyl}piperazineHCID 4424288683%

반응 조건

온도-20 °C

반응 단계

A stirred solution of 1-benzyl-4-(4-nitrophenyl)piperazine (5.95 g, 20.0 mmol) and chloromethylphenylsulfone (3.82 g, 20.0 mmol) in dry THF under nitrogen at −60° C. is treated with 1.0M KO-t-Bu in THF (44.0 mL, 44.0 mmol), warmed to −20° C. over a 1 h period, quenched with acetic acid and treated sequentially with water, saturated aqueous NaHCO3 and ether. The phases are separated and the aqueous phase is extracted with ether. The combined ethers are washed with water and brine, dried over MgSO4 and concentrated in vacuo. The resultant residue is chromatographed (silica gel, 1:1 and 1:0 ethyl acetate:hexanes as eluent) to give the title compound as a yellow solid, 7.52 g (83% yield), mp 145-146° C., characterized by NMR and mass spectral analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560470B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-a74a25ab7e974c9e9b47fde5425c2c4f
출처 메모uspto-grants-2009_07