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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1413166생성일: 2026년 10월 25일

Methyl Ethyl Ketone → N-(1-ethyl-2-pyrrolidylmethyl)-8-methoxy-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/reaction/1413166

반응식

참여 물질

역할이름HCID투입량
반응물Methyl Ethyl KetoneHCID 6569—
반응물2-Aminomethyl-1-ethylpyrrolidineHCID 117295—
반응물8-Methoxy-1,4-benzodioxane-5-carbonyl chlorideHCID 20544710—
용매WaterHCID 962—
생성물N-(1-ethyl-2-pyrrolidylmethyl)-8-methoxy-1,4-benzodioxane-5-carboxamideHCID 53981082103.4%

반응 단계

87 g of 1-ethyl-2-aminomethyl pyrrolidine and 775 cm3 of methyl ethyl ketone were introduced into a balloon flask provided with an agitator and a thermometer and then, in portions, 155 g of 8-methoxy-1,4-benzodioxane-5-carbonyl chloride was added, with the temperature being maintained at from 5°-10° C. After agitation the mixture was dissolved with 1,500 cm3 of water and then the methyl ethyl ketone was distilled. The remaining solution was filtered and then treated with sodium hydroxide. The oil was decanted and then extracted with methylene chloride. The solution was dried on potassium carbonate and then the methylene chloride was distilled under vacuum. 224.5 g of N-(1-ethyl-2-pyrrolidylmethyl)-8-methoxy-1,4-benzodioxane-5-carboxamide was produced. 197.5 g of the base produced was dissolved in 760 cm3 of absolute alcohol, and then 67 g of oxalic acid in solution in 195 cm3 of absolute alcohol was added. The crystals formed were dried off, washed with absolute alcohol and then dried. 208.5 g of N-(1-ethyl-2-pyrrolidylmethyl)-8-methoxy-1,4-benzodioxane-5-carboxamide oxalate was produced (M.P. 129°-130° C.; yield: 82%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04248885
출처 데이터셋uspto-grants-1981_02
ORD IDord-1a9aeacbacac403eaa427a532c4b504b
출처 메모uspto-grants-1981_02