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HRID 1382154作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物(2,4-Dichloro-5-(1-methylethoxy)phenyl)hydrazineHCID 170281—
反応物Ethyl difluoroacetylcarbamateHCID 14392483—
溶媒O-XyleneHCID 7237—
生成物1-[2,4-dichloro-5-(1-methylethoxy)phenyl]-3-difluoromethyl-4,5-dihydro-1,2,4-triazol-5(1H)-oneHCID 13574510348.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04806145
出典データセットuspto-grants-1989_02
ORD IDord-4b9928f8a63d4fdfabaae0a9e8a0be4e
出典メモuspto-grants-1989_02