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HRID 916859作成日:2026年10月27日

Nitrogen → (2,6-Dimethoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)phenyl]-methanone

https://huagongshe.com/reaction/916859

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物2,6-DimethoxynaphthaleneHCID 79627—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物4-(2-(Piperidin-1-yl)ethoxy)benzoyl chlorideHCID 11119066—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(2,6-Dimethoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)phenyl]-methanoneHCID 1165466068%

反応条件

温度0 °C

反応手順

In a dry round bottom flask equipped with stir bar, temperature probe and N2 line, dissolve 2,6-dimethoxynaphthalene (1.0 eq) in CH2Cl2 (5 volume equivalents) at ambient temperature. Cool the solution to 0° C. in with an ice bath, and add 4-(2-piperidin-1-yl-ethoxy)-benzoyl chloride (1.1 eq). Add aluminum chloride (2.0 eq). Once the reaction is determined to be complete, quench the reaction slowly with 1 N NaOH and dilute with additional water and CH2Cl2. Wash the aqueous layer with (1×20 mL) of CH2Cl2. Combine the organic extracts and wash with brine and dry (Na2SO4). Recrystallize the crude product from methanol to give (2,6-dimethoxy-naphthalen-1-yl)[4(2-piperidin-1-yl-ethoxy)-phenyl]-methanone (average yield 68%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07271264B2
出典データセットuspto-grants-2007_09
ORD IDord-3d8ec612189a4600be88781b87d7df3d
出典メモuspto-grants-2007_09