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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (4-Chloro-2-fluoro-5-propan-2-yloxyphenyl)hydrazine | HCID 185080 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | 1,1-Dibromo-3,3,3-trifluoroacetone | HCID 550523 | — |
| 반응물 | Ethyl 3-(triphenyl-lambda~5~-phosphanylidene)propanoate | HCID 12607919 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2-(2-Fluoro-4-chloro-5-isopropoxyphenyl)-4-methyl-5-trifluoromethylpyridazin-3-one | HCID 11089828 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06218338B1 |
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| 출처 데이터셋 | uspto-grants-2001_04 |
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| ORD ID | ord-4c56b8cd4c0d4cbdaaa92068ee2b995b |
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| 출처 메모 | uspto-grants-2001_04 |
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