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HRID 748934생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/748934

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물2,6-DimethoxynaphthaleneHCID 79627—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물4-(2-(Piperidin-1-yl)ethoxy)benzoyl chlorideHCID 11119066—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(2,6-Dimethoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)phenyl]-methanoneHCID 11654660—

반응 조건

온도0 °C

반응 단계

Dissolve 2,6-dimethoxynaphthalene (1.0 eq.) in CH2Cl2 (5 volume eq.) at ambient temperature in a dry round bottom flask equipped with stir bar, temperature probe and N2 line. Cool the solution to 0° C. 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 CH2Cl2 (20 mL). 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07399867B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-03b230a1ea134a60b8fda28f8e336702
출처 메모uspto-grants-2008_07