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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1375223생성일: 2026년 10월 25일

Tetrabutylammonium Fluoride → 2-(4-Chlorophenyl)-N-(4'-hydroxy-3'-methoxy-biphenyl-2-yl)-2-prop-2-ynyloxy-acetamide

https://huagongshe.com/reaction/1375223

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물N-[4'-(tert-butyl-diphenyl-silanyloxy)-3'-methoxy-biphenyl-2-yl]-2-(4-chlorophenyl)-2-prop-2-ynyloxy-acetamideHCID 21079853—
용매DichloromethaneHCID 6344—
생성물2-(4-Chlorophenyl)-N-(4'-hydroxy-3'-methoxy-biphenyl-2-yl)-2-prop-2-ynyloxy-acetamideHCID 21079850—

반응 단계

A solution of 10.2 g (15.5 mmol) N-[4′-(tert-butyl-diphenyl-silanyloxy)-3′-methoxy-biphenyl-2-yl]-2-(4-chlorophenyl)-2-prop-2-ynyloxy-acetamide and 24.5 g (77.5 mmol) tetrabutylammonium fluoride in 200 ml of dichloromethane is stirred for 4 hours at room temperature. After extracting with water/ethyl acetate and evaporation of the organic phase, the residue is subjected to flash-chromatography (ethyl acetate/hexane 4:6). Yield: 2-(4-chlorophenyl)-N-(4′-hydroxy-3′-methoxy-biphenyl-2-yl)-2-prop-2-ynyloxy-acetamide, m.p. 140–142° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07166746B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-2d23ba3080534274a942c4ce53d85812
출처 메모uspto-grants-2007_01