Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1382154생성일: 2026년 10월 26일
Phosphorus oxide (P4O10) → 1-[2,4-dichloro-5-(1-methylethoxy)phenyl]-3-difluoromethyl-4,5-dihydro-1,2,4-triazol-5(1H)-one
https://huagongshe.com/reaction/1382154
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphorus oxide (P4O10) | HCID 14812 | — |
| 반응물 | (2,4-Dichloro-5-(1-methylethoxy)phenyl)hydrazine | HCID 170281 | — |
| 반응물 | Ethyl difluoroacetylcarbamate | HCID 14392483 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 1-[2,4-dichloro-5-(1-methylethoxy)phenyl]-3-difluoromethyl-4,5-dihydro-1,2,4-triazol-5(1H)-one | HCID 135745103 | 48.5% |
반응 단계
To a stirred solution of 11.8 g (0.05 mole) of 2,4-dichloro-5-(1-methylethoxy)phenylhydrazine and 10.0 g (0.06 mole) of ethyl difluoroacetylcarbamate in 130 mL of xylene was added 2.5 g (0.02 mole) of phosphorus pentoxide. After complete addition the mixture was heated at reflux for 1.5 hours then allowed to cool to room temperature for approximately 18 hours. The reaction mixture was decanted from a dark residue in the reaction flask and washed with water. The washed mixture was extracted with a 10% aqueous sodium hydroxide solution. The basic extract was made acidic with concentrated hydrochloric acid to form an oily precipitate. This aqueous phase was decanted from the oily residue and fresh water added to wash the residue. This residue was dissolved in 160 mL of methylene chloride and filtered through a celite pad. The filtrate was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to leave a semi-solid residue. The residue was triturated with approximately 125 mL of petroleum ether to provide 8.2 g of 1-[2,4-dichloro-5-(1-methylethoxy)phenyl]-3-difluoromethyl-4,5-dihydro-1,2,4-triazol-5(1H)-one.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04806145 |
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| 출처 데이터셋 | uspto-grants-1989_02 |
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| ORD ID | ord-4b9928f8a63d4fdfabaae0a9e8a0be4e |
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| 출처 메모 | uspto-grants-1989_02 |
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