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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 414245생성일: 2026년 10월 25일

Hydrogen Bromide → 3-[4-[4-(4-Hydroxyphenyl)-1-piperazinyl]phenyl]-5,5-dimethyl-1-(1-methyl-2-oxopropyl)-2,4-imidazolidinedione

https://huagongshe.com/reaction/414245

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물Disodium disulfiteHCID 24346—
반응물3-[4-[4-(4-Methoxyphenyl)-1-piperazinyl]phenyl]-5,5-dimethyl-1-(1-methyl-2-oxopropyl)-2,4-imidazolidinedioneHCID 21281909—
용매WaterHCID 962—
생성물3-[4-[4-(4-Hydroxyphenyl)-1-piperazinyl]phenyl]-5,5-dimethyl-1-(1-methyl-2-oxopropyl)-2,4-imidazolidinedioneHCID 1512555186%

반응 단계

A mixture of 25.6 parts of 3-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-5,5-dimethyl-1-(1-methyl-2-oxopropyl)-2,4-imidazolidinedione, 3 parts of sodium disulfite and 375 parts of a hydrobromic acid solution 48% in water was stirred for 6 hours at reflux temperature. After cooling. the crystallized product was filtered off, washed with 2-propanone and suspended in a mixture of water, trichloromethane and 1-butanol. The whole was treated with potassium carbonate (pH 8~9). The separated organic layer was set aside and the aqueous phase was extracted twice with the same mixture. The combined extracts (see above) were evaporated in vacuo. The residue was crystallized from 1-butanol. The product was filtered off and dried, yielding 21.3 parts (86%) of 3-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]-5,5-dimethyl-1-(1-methyl-2-oxopropyl)-2,4-imidazolidinedione; mp. 225.9° C. (intermediate 21).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04791111
출처 데이터셋uspto-grants-1988_12
ORD IDord-302aa818216140e9ac0ca3dd19cd0fbc
출처 메모uspto-grants-1988_12