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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 461465생성일: 2026년 10월 26일

Dimethylformamide → N-(N-[Bicyclo[2.2.1]hept-2-en-5-ylmethyl]carbamoyl)-2-phenylethenesulfonamide

https://huagongshe.com/reaction/461465

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물2-PhenylethenesulfonamideHCID 257501—
반응물N'-(bicyclo[2.2.1]hept-5-en-2-ylmethyl)-N,N-diphenylureaHCID 12282081—
용매Diethyl EtherHCID 3283—
생성물N-(N-[Bicyclo[2.2.1]hept-2-en-5-ylmethyl]carbamoyl)-2-phenylethenesulfonamideHCID 54231290—

반응 단계

To a solution of 1.8 g. of 2-phenylethenesulfonamide and 4.8 g. of 1,1-diphenyl-3-(bicyclo[2.2.1]hept-2-en-5-ylmethyl)urea in 20 ml. of N,N-dimethylformamide, is added, with stirring 0.64 g. of a 56.6% dispersion of sodium hydride in mineral oil. The mixture is stirred at ambient temperature overnight, during which time a heavy precipitate forms. To the reaction mixture is then added 200 ml. of ether. After stirring for 15 minutes, the precipitate is filtered off. It is dissolved in 50 ml. of water, and then the crude product is precipitated by acidification usng concentrated hydrochloric acid. It is filtered off and recrystallized from aqueous acetone. The yield is 1.9 g. (56%) of a solid, m.p. 161°-163.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04062960
출처 데이터셋uspto-grants-1977_12
ORD IDord-0f04b68366f946ca8929ad0918755bef
출처 메모uspto-grants-1977_12