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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36444생성일: 2026년 10월 25일

Triethylamine → 1-(2-Chlorophenyl)-4-{2-[bis(4-hydroxyphenyl)methyl]benzyl}piperazine

https://huagongshe.com/reaction/36444

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(2-Chlorophenyl)piperazineHCID 415628—
반응물2-[Bis(4-hydroxyphenyl)methyl]benzylbromideHCID 19938176—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Chlorophenyl)-4-{2-[bis(4-hydroxyphenyl)methyl]benzyl}piperazineHCID 1993811814.6%

반응 단계

In 50 ml of tetrahydrofuran were dissolved 1.5 g of 1-(2-chlorophenyl)piperazine and 5 ml of triethylamine, and 3.4 g of 2-[bis(4-hydroxyphenyl)methyl]benzylbromide was added thereto. The mixture was heated under reflux for 3.5 hours, and then insoluble substances were filtered off. The filtrate was concentrated, and the residue was subjected to extraction with the addition of water and ethyl acetate. The organic layer was separated, and the aqueous layer was then extracted with ethyl acetate. The organic layers were combined and then dried over anhydrous magnesium sulfate. The solvent was evaporated off under reduced pressure, and the residue was purified by silica gel chromatography to afford 0.54 g of the desired compound (Compound 89).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05413997
출처 데이터셋uspto-grants-1995_05
ORD IDord-0208c64273a84e8e8c4fda96508a2f39
출처 메모uspto-grants-1995_05