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HRID 602164作成日:2026年10月26日

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

https://huagongshe.com/reaction/602164

反応式

関与物質

役割名称HCID仕込み量
反応物PhthalimideHCID 6809—
反応物TriphenylphosphineHCID 11776—
反応物Methyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoateHCID 58992598—
反応物Diethylazodicarboxylate tolueneHCID 66777355—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物N-[[1-[2-(Methoxycarbonyl)phenyl]piperidin-3-yl]methyl]phthalimideHCID 5899269195%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902367B2
出典データセットuspto-grants-2011_03
ORD IDord-0cc93c605ff844d78e7a84d99a0d7f4f
出典メモuspto-grants-2011_03