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HRID 1711981作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Perfluoro-1-butanesulfonyl fluorideHCID 67814—
反応物DiisopropylethylamineHCID 81531—
反応物7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-olHCID 136352503—
溶媒DichloromethaneHCID 6344—
生成物Perfluoro-1-butanesulfonic acid 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl)-naphthalen-2-yl esterHCID 8660215583.3%

反応条件

温度23 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07790882B2
出典データセットuspto-grants-2010_09
ORD IDord-7d724ff8c31f48fe9d5c48914b96e1c2
出典メモuspto-grants-2010_09