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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Perfluoro-1-butanesulfonyl fluoride | HCID 67814 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-ol | HCID 136352503 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Perfluoro-1-butanesulfonic acid 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl)-naphthalen-2-yl ester | HCID 86602155 | 83.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07790882B2 |
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| 출처 데이터셋 | uspto-grants-2010_09 |
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| ORD ID | ord-7d724ff8c31f48fe9d5c48914b96e1c2 |
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| 출처 메모 | uspto-grants-2010_09 |
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