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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1711981생성일: 2026년 10월 26일

Perfluoro-1-butanesulfonyl fluoride → Perfluoro-1-butanesulfonic acid 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl)-naphthalen-2-yl ester

https://huagongshe.com/reaction/1711981

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참여 물질

역할이름HCID투입량
반응물Perfluoro-1-butanesulfonyl fluorideHCID 67814—
반응물DiisopropylethylamineHCID 81531—
반응물7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-olHCID 136352503—
용매DichloromethaneHCID 6344—
생성물Perfluoro-1-butanesulfonic acid 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl)-naphthalen-2-yl esterHCID 8660215583.3%

반응 조건

온도23 °C

반응 단계

A solution of 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-ol (1.0 g, 2.4 mmol) in diisopropylethylamine (0.94 ml, 7.1 mmol) and dichloromethane (35 ml) was treated with N,N-dimethylaminopyridine (DMAP, 50 mg, 0.41 mmol) at 0° C. Then perfluoro-1-butanesulfonyl fluoride (0.51 ml, 2.8 mmol) was added dropwise and the resulting solution was stirred for 19 hrs at 23° C. The resulting solution was quenched with sat. aqueous ammonium chloride solution. The organic layer was separated and the water layer was extracted twice with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (hexane/EtOAc 3:1) to give 1.4 g (2.0 mmol) of the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790882B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-7d724ff8c31f48fe9d5c48914b96e1c2
출처 메모uspto-grants-2010_09