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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1197778생성일: 2026년 10월 26일

Ethanol → 4-Chloro-5-hydroxy-2-(phenylmethyl)-3(2H)-pyridazinone

https://huagongshe.com/reaction/1197778

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Potassium HydroxideHCID 14797—
반응물2-Benzyl-4,5-dichloro-2,3-dihydropyridazin-3-oneHCID 722438—
용매WaterHCID 962—
생성물4-Chloro-5-hydroxy-2-(phenylmethyl)-3(2H)-pyridazinoneHCID 54683180—

반응 단계

To the mixture of 60 g of 2-benzyl-4,5-dichloro-3(2H)-pyridazinone and 38.8 g of potassium hydroxide was added 250 ml of ethanol and 150 ml of water and heated in an oil bath to the refluxing temperature for 10 hours. After reaction the solvent was distilled off under reduced pressure, and to the residual solution was added 200 ml of water and washed twice with chloroform, the water layer was acidified with concentrated hydrochloric acid. The white solid thus separated was filtered off, washed with water and dried to obtain 55 g of 2-benzyl-4-chloro-5-hydroxy-3(2H)-pyridazinone. Subsequently, in aqueous sodium hydroxide solution (NaOH 1.82 g, water 20 ml) were added 5.0 g of 2-benzyl-4-chloro-5-hydroxy-3(2H)-pyridazinone and 200 mg of 5 % Pd/C , then 474 ml of hydrogen gas was absorbed in the solution under normal pressure. After reaction, Pd/C was filtered off and to the solution was added concentrated hydrochloric acid to be acidified. The white solid thus separated was filtered off, washed with water and dried to obtain 4.1 g of 2-benzyl-5-hydroxy-3(2H)-pyridazinone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05278163
출처 데이터셋uspto-grants-1994_01
ORD IDord-efd3a1815306411fbd3775da2212ce53
출처 메모uspto-grants-1994_01