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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1283972생성일: 2026년 10월 25일

Ethanol → N-benzyl-N-(3,4-dibenzyloxybenzoyl)methyl-2-(4-acetamidophenoxy)ethylamine

https://huagongshe.com/reaction/1283972

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물3,4-Dibenzyloxyphenacyl bromideHCID 12681802—
반응물N-[2-(4-acetamidophenoxy)ethyl]benzylamineHCID 22750197—
용매IsopropanolHCID 3776—
생성물N-benzyl-N-(3,4-dibenzyloxybenzoyl)methyl-2-(4-acetamidophenoxy)ethylamineHCID 2275018166.9%

반응 단계

A mixture of 3,4-dibenzyloxyphenacyl bromide (32.8 g.), N-[2-(4-acetamidophenoxy)ethyl]benzylamine (22.8 g.), anhydrous sodium carbonate (8.4 g.) and ethanol (1 liter) was boiled under reflux for 2 hours, then filtered hot to remove the inorganic sediment and evaporated in vacuo to afford a thick syrup. The latter was dissolved in hot isopropanol and the solution cooled, the precipitated solid then being collected by filtration. To a hot solution of the solid in fresh isopropanol were added a few milliliters of ethyl acetate, and the solution was then allowed to cool to room temperature. The crystallized solid was collected by filtration, washed in diethyl ether and dried. Recrystallization from an isopropanol/ethyl acetate mixture afforded N-benzyl-N-(3,4-dibenzyloxybenzoyl)methyl-2-(4-acetamidophenoxy)ethylamine (32.8 g.), m.p. 104°-6°C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03976783
출처 데이터셋uspto-grants-1976_08
ORD IDord-740ae0bab8e74bfba8f48ec6ad15daaa
출처 메모uspto-grants-1976_08