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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 972679생성일: 2026년 10월 25일

Sodium Hydroxide → 3'-Chloro-4'-(4-methyl-1-piperazinyl)acetophenone

https://huagongshe.com/reaction/972679

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물1-MethylpiperazineHCID 53167—
반응물Ethanone, 1-(3,4-dichlorophenyl)-HCID 75841—
용매WaterHCID 962—
생성물3'-Chloro-4'-(4-methyl-1-piperazinyl)acetophenoneHCID 21404580—

반응 단계

3',4'-Dichloroacetophenone (9.65 g., 0.05 mole) and N-methylpiperazine (10 g., 0.1 mole) are refluxed (165° C.) for 24 hours. The solution is cooled and 100 ml. water containing 2 g. of sodium hydroxide is added. The oil is decanted and diluted with 200 ml. of toluene and washed first with dilute alkali then several times with water. The toluene layer is dried with magnesium sulfate and evaporated in vacuo to an oil. The residue is distilled 146°-150° at 0.1-0.3 mm., yield 3.0 g. This product is dissolved in ethyl ether and converted to the hydrochloride using isopropanolic hydrogen chloride and the salt crystallized from acetonitrile. The purified salt is reconverted to the base with dilute sodium hydroxide. The product is extracted using ethyl ether, separated, dried, evaporated to dryness to give 3'-chloro-4'-(4-methyl-1-piperazinyl)acetophenone as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04053470
출처 데이터셋uspto-grants-1977_10
ORD IDord-0b4d76a994e04d15b9d3ca5c9f0601d9
출처 메모uspto-grants-1977_10