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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1711981Erstellt: 25. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPerfluoro-1-butanesulfonyl fluorideHCID 67814—
EduktDiisopropylethylamineHCID 81531—
Edukt7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-olHCID 136352503—
LösungsmittelDichloromethaneHCID 6344—
ProduktPerfluoro-1-butanesulfonic acid 7-methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl)-naphthalen-2-yl esterHCID 8660215583,3%

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07790882B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-7d724ff8c31f48fe9d5c48914b96e1c2
Quellennotizuspto-grants-2010_09