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HRID 605780作成日:2026年10月26日

Triphenylphosphine → Tert-butyl 4-[(6-chloropyridin-2-yl)oxy]piperidine-1-carboxylate

https://huagongshe.com/reaction/605780

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
反応物6-chloropyridin-2-olHCID 178516025—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 4-[(6-chloropyridin-2-yl)oxy]piperidine-1-carboxylateHCID 2190605878.7%

反応手順

Diethyl azodicarboxylate (11 ml, 40% Tol solution) was dropwise added to a THF (30 ml) solution containing tert-butyl 4-hydroxypiperidine-1-carboxylate (4.6 g), triphenylphosphine (6.1 g) and 6-chloro-2-pyridinol (2.0 g) at 0° C., followed by stirring at room temperature for 24 hours. Water was added to the reaction solution, followed by extraction with EtOAc. The organic layer was washed with an aqueous 1 M sodium hydroxide solution, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: hexane:EtOAc=10:1 (v/v)) to obtain tert-butyl 4-[(6-chloro-2-pyridinyl)oxy]-1-piperidinecarboxylate (3.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915261B2
出典データセットuspto-grants-2011_03
ORD IDord-c83ebe610a2f44f386f913232eae4cd8
出典メモuspto-grants-2011_03