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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 269916생성일: 2026년 10월 27일

Tetrahydrofuran → 1-(2,5-Difluoro-4-methoxyphenyl)-4-methoxymethylenepiperidine

https://huagongshe.com/reaction/269916

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
반응물1-(2,5-Difluoro-4-methoxyphenyl)piperidin-4-oneHCID 23111466—
용매WaterHCID 962—
생성물1-(2,5-Difluoro-4-methoxyphenyl)-4-methoxymethylenepiperidineHCID 2311140034.1%

반응 단계

A reaction vessel was charged with methoxymethyltriphenyl-phosphonium chloride (1.114 g), the atomosphere indide the vessel was substituted with nitrogen, and anhydrous tetrahydrofuran (2 mL) was added, followed by further dropwise addition of 1.57 M n-butyl lithium-in-hexane solution (2 mL) at room temperature and thereafter 10 minutes' stirring at room temperature. To the reaction mixture a mixture of 1-(2,5-difluoro-4-methoxyphenyl)piperidin-4-one (676 mg) and anhydrous tetrahydrofuran (0.5 mL) was added dropwise, followed by 30 minutes' stirring at room temperature. To the reaction mixture water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline solution and dried over anhydrous sodium sulfate. Distilling the solvent off, the crude product as obtained was purified on silica gel column chromatography (eluent, hexane: ethyl acetate=10:1) to provide 1-(2,5-difluoro-4-methoxyphenyl)-4-methoxymethylenepiperidine (257 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449466B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-0354f4e12ffe4f7cad2355f89c6f816a
출처 메모uspto-grants-2008_11