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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27165생성일: 2026년 10월 25일

Dimethylformamide → N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamide

https://huagongshe.com/reaction/27165

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Benzyl chloroformateHCID 10387—
반응물Potassium CarbonateHCID 11430—
반응물N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(p-toluidino)acetamideHCID 10042154—
용매ChloroformHCID 6212—
생성물N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamideHCID 2046050984.8%

반응 단계

A mixture of N-[2(3,4-dimethoxyphenyl)ethyl]2-(p-toluidino)acetamide (3.6 g) and anhydrous potassium carbonate (2.5 g) was added to anhydrous dimethylformamide (25 ml). The mixture was vigorously stirred under ice cooling and to the solution was dropwise added over 20 minutes an anhydrous chloroform solution (5 ml) containing benzyl chloroformate (2.04 g). The reaction mixture was poured into ice-water and extracted with chloroform. The extract was washed with water, dried and the solvent was distilled off. The residue was crystallized by treating with ether to give N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(N-benzyloxycarbonyl-p-toluidino)-acetamide (4.3 g), mp 81° to 85° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04220647
출처 데이터셋uspto-grants-1980_09
ORD IDord-5a341a5ba17e4d23a8c6da3051bc6881
출처 메모uspto-grants-1980_09