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HRID 2106780생성일: 2026년 10월 25일

Pyridine → N-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]acetamide

https://huagongshe.com/reaction/2106780

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DimethylformamideHCID 6228—
반응물Acetyl chlorideHCID 6367—
반응물4-[4-(4-Aminophenyl)piperazin-1-yl]phenolHCID 10221065—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물N-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]acetamideHCID 1512549742.5%

반응 단계

To a stirred solution of 10.8 parts of 4-[4-(4-aminophenyl)-1-piperazinyl]phenol in 3.2 parts of pyridine and 90 parts of N,N-dimethylformamide was added dropwise a solution of 3.1 parts of acetyl chloride in 27 parts of methylbenzene at 20° C. (exothermic reaction). Upon completion, stirring was continued for 1 hour at 20° C. The reaction mixture was poured into water while stirring. The product was filtered off, washed with water and dissolved in a mixture of trichloromethane and methanol (3:1 by volume). The whole was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The second fraction was collected and the eluent was evaporated. The residue was crystallized from a mixture of ethanol and methylbenzene (1:1 by volume)+(activated charcoal). The produce was filtered off and dried yielding 5.3 parts (42.5%) of N-[4-[4-(4-hydroxyphenyl)-1-piperazinyl]phenyl]acetamide; mp. 256.2° C. (compound 1.03).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04931444
출처 데이터셋uspto-grants-1990_06
ORD IDord-ba3575adee5644449488737b02f2352a
출처 메모uspto-grants-1990_06