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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 648487생성일: 2026년 10월 23일

1,4-Dioxane → HCID 14152935, 화합물

https://huagongshe.com/ko/reaction/648487

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물Ethyl 2-((propan-2-yl)amino)acetateHCID 351625—
반응물Phenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamateHCID 981607—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
생성물HCID 14152935HCID 1415293573%

반응 단계

A mixture of 5 parts of phenyl[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]carbamate, 3 parts of ethyl[(1-methylethyl)amino]acetate, 1 part of N,N-dimethyl-4-pyridinamine and 100 parts of 1,4-dioxane was stirred and refluxed overnight. The warm solution was saturated with water and allowed to cool. The solution was poured onto water and extracted with trichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by filtration over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The filtrate was evaporated and the residue was crystallized from methylbenzene, yielding 3.7 parts (73%) of 3-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-1-(1-methylethyl)-2,4-imidazolidinedione; mp. 193.7° C. (38).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04735942
출처 데이터셋uspto-grants-1988_04
ORD IDord-be92ae4a412444b888a6a9a14e4eb534
출처 메모uspto-grants-1988_04