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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127406생성일: 2026년 10월 26일

Chloroform → N-(1-allyl-2-pyrrolidylmethyl)-7-ethylsulfonyl-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/reaction/127406

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물1-(Allyl)pyrrolidine-2-methylamineHCID 117296—
반응물7-Ethylsulfonyl-1,4-benzodioxane-5-carbonyl chlorideHCID 20544728—
용매WaterHCID 962—
생성물N-(1-allyl-2-pyrrolidylmethyl)-7-ethylsulfonyl-1,4-benzodioxane-5-carboxamideHCID 2483493593.4%

반응 단계

58 g of 1-allyl-2-aminomethyl-pyrrolidine and 360 ml of chloroform were introduced into a balloon flask provided with an agitator and a thermometer and then, with the temperature being maintained at 5°-10° C., 120 g of 7-ethylsulfonyl-1,4-benzodioxane-5-carbonyl chloride was added. After agitation of the mixture and the addition of a liter of water, the chloroform was distilled. The resulting solution was filtered on carbon black and then the base was precipitated by the addition of 40 ml of 30% soda lye. The resulting crystals were dried off, washed with water and then dried. 152 g of N-(1-allyl-2-pyrrolidylmethyl)-7-ethylsulfonyl-1,4-benzodioxane-5-carboxamide was produced (M.P.: 78°-80° C.; yield: 93.4%). 146 g of the resulting base was dissolved hot in 290 ml of absolute alcohol, and then the solution was filtered on carbon black and acidified by the addition of a solution of 13.5 g of hydrochloric acid in 100 ml of absolute alcohol. After cooling the crystals formed were dried off, washed with absolute alcohol and dried and then purified by recrystallization from absolute alcohol. 119.5 g of N-(1-allyl-2-pyrrolidylmethyl)-7-ethylsulfonyl-1,4-benzodioxane-5-carboxamide hydrochloride was produced (M.P.: 138°-140° C.; yield: 75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255580
출처 데이터셋uspto-grants-1981_03
ORD IDord-d991ef54ee38453ead272a4def54c546
출처 메모uspto-grants-1981_03