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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1711980생성일: 2026년 10월 26일

Sodium hydride → 7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-ol

https://huagongshe.com/reaction/1711980

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-Phenylethanol, (R)-HCID 637516—
반응물1-(4-Chlorophthalazin-1-yl)-7-methoxynaphthalen-2-olHCID 136343453—
용매TetrahydrofuranHCID 8028—
생성물7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-olHCID 13635250386.7%

반응 단계

To a suspension of sodium hydride (0.80 g, 33 mmol) in tetrahydrofuran (80 ml) was added a solution of (R)-phenylethanol (2.0 g, 17 mmol) in tetrahydrofuran (3 ml) cautiously over 10 min at 23° C. The mixture was stirred for 15 min, then 1-(4-chlorophthalazin-1-yl)-7-methoxy-naphthalen-2-ol (5.1 g, 15 mmol) was added portionwise. The resulting red suspension was stirred for 20 hrs at 23° C., then the solvent was removed under reduced pressure. The residue was dissolved in dichloromethane and poured into brine. The organic layer was separated and the aqueous layer was extracted two times 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 4:1 to 1:1) to give 5.5 g (13 mmol) of the title compound as a 1:1 mixture of diastereomers, as a white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790882B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-984b8e45f7044bec9fc262c677bde064
출처 메모uspto-grants-2010_09