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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1262925생성일: 2026년 10월 26일

Hydroxyphenylacetic acid → Chloridazon

https://huagongshe.com/reaction/1262925

반응식

참여 물질

역할이름HCID투입량
반응물Hydroxyphenylacetic acidHCID 127—
반응물AmmoniaHCID 222—
반응물4,5-Dichloro-2-phenyl-3(2H)-pyridazinoneHCID 72813—
생성물ChloridazonHCID 15546—

반응 단계

4,5-Dichloro-2-phenyl-pyridazinone (2.41 g), 4-hydroxyphenyl-acetic acid (1.0 g) and 20% aqueous ammonia (20 ml) were heated to 100°-110° C. with stirring in a small autoclave for 4 hours. The reaction mixture was then cooled to room temperature, and the resulting precipitate of 4-chloro-5-amino-2-phenyl-3(2H)-pyridazinone was isolated by filtration, washed with water and dried. 1.86 g of pure 4-chloro-5-amino-2-phenyl-3(2H)-pyridazinone were obtained, m.p. 206°-207° C. The mother liquor and the washings contained 0.15 g of 4-chloro-5-amino-2-phenyl-3(2H)-pyridazinone. The total amount of 4-chloro-5-amino-2-phenyl-3(2H)-pyridazinone formed was thus 2.01 g (91%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04454318
출처 데이터셋uspto-grants-1984_06
ORD IDord-2b94027f30854d7db2fd3abe8b63abd7
출처 메모uspto-grants-1984_06