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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

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물(2,4-Dichloro-5-(1-methylethoxy)phenyl)hydrazineHCID 170281—
반응물Ethyl difluoroacetylcarbamateHCID 14392483—
용매O-XyleneHCID 7237—
생성물1-[2,4-dichloro-5-(1-methylethoxy)phenyl]-3-difluoromethyl-4,5-dihydro-1,2,4-triazol-5(1H)-oneHCID 13574510348.5%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04806145
출처 데이터셋uspto-grants-1989_02
ORD IDord-4b9928f8a63d4fdfabaae0a9e8a0be4e
출처 메모uspto-grants-1989_02