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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324255생성일: 2026년 10월 23일

(4-Chloro-2-fluoro-5-propan-2-yloxyphenyl)hydrazine → 2-(2-Fluoro-4-chloro-5-isopropoxyphenyl)-4-methyl-5-trifluoromethylpyridazin-3-one

https://huagongshe.com/ko/reaction/324255

반응식

참여 물질

역할이름HCID투입량
반응물(4-Chloro-2-fluoro-5-propan-2-yloxyphenyl)hydrazineHCID 185080—
반응물Sodium AcetateHCID 517045—
반응물1,1-Dibromo-3,3,3-trifluoroacetoneHCID 550523—
반응물Ethyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoateHCID 12607919—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물2-(2-Fluoro-4-chloro-5-isopropoxyphenyl)-4-methyl-5-trifluoromethylpyridazin-3-oneHCID 11089828—

반응 조건

온도70 °C

반응 단계

To a solution of 5.3 g (53.3 mmol) of sodium acetate mixed with about 100 ml of water was added under ice cooling 6.6 g (24.3 mmol) of 1,1-dibromo-3,3,3-trifluoroacetone, and the mixture was stirred at 70° C. for 20 minutes. The reaction mixture was cooled to room temperature, to which a solution of 5.8 g (21.5 mmol) of 2-fluoro-4-chloro-5-isopropoxyphenylhydrazine dissolved in about 20 ml of diethyl ether was added, and the mixture was stirred at room temperature for 1 hour. The ether layer was separated and then concentrated. About 60 ml of tetrahydrofuran (hereinafter referred to as THF) was added to the residue, to which 8.3 g (23.0 mmol) of (carbethoxyethylidene)triphenylphosphorane was added, and the mixture was heated under reflux for 2 hours. The THF was distilled out under reduced pressure, and the residue was subjected to silica gel column chromatography, which afforded 3.8 g (10.5 mmol) of 2-[2-fluoro-4-chloro-5-isopropoxyphenyl]-4-methyl-5-trifluoromethylpyridazin-3-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218338B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-4c56b8cd4c0d4cbdaaa92068ee2b995b
출처 메모uspto-grants-2001_04