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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602164생성일: 2026년 10월 25일

Phthalimide → N-[[1-[2-(Methoxycarbonyl)phenyl]piperidin-3-yl]methyl]phthalimide

https://huagongshe.com/reaction/602164

반응식

참여 물질

역할이름HCID투입량
반응물PhthalimideHCID 6809—
반응물TriphenylphosphineHCID 11776—
반응물Methyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoateHCID 58992598—
반응물Diethylazodicarboxylate tolueneHCID 66777355—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물N-[[1-[2-(Methoxycarbonyl)phenyl]piperidin-3-yl]methyl]phthalimideHCID 5899269195%

반응 단계

Triphenylphosphine (1.68 g, 6.20 mmol) and phthalimide (799 mg, 5.43 mmol) were added to methyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoate (1.29 g, 5.17 mmol) in tetrahydrofuran (10 mL). The reaction mixture was stirred at room temperature for 10 min and a 40% diethyl azodicarboxylate/toluene solution (3.52 mL, 7.76 mmol) was added. The mixture was then stirred at room temperature for 8 hours. Subsequently, water was added and the mixture was extracted with ethylacetate. The extract was washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=20:1->5:1) gave 1.85 g (95%) of the desired compound as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902367B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-0cc93c605ff844d78e7a84d99a0d7f4f
출처 메모uspto-grants-2011_03