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HRID 1163856作成日:2026年10月24日

Pyridine → 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-2-yl)-2-butyl chloroformate

https://huagongshe.com/ja/reaction/1163856

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物PhosgeneHCID 6371—
反応物TriadimenolHCID 41368—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-2-yl)-2-butyl chloroformateHCID 86738718—

反応手順

To a solution of 29.6 g (0.1 mole) of 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol in 250 ml of THF was added 20 ml of liquid phosgene, followed by 9 ml of pyridine. The mixture was stirred at ambient temperature for about 21 hours. White solid (water-soluble) was filtered off and the THF filtrate concentrated in vacuum to a residual oil, the intermediate chloroformate. Further purification of the chloroformate was accomplished by dissolving it in about 300 ml of 1-chlorobutane, washing the butyl chloride solution with 0.5 N HCl (twice), water and saturated brine, drying (MgSO4), filtration, and evaporation of the filtrate in vacuum to leave, as a residual oil, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-2-yl)-2-butyl chloroformate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04367089
出典データセットuspto-grants-1983_01
ORD IDord-9c84bd54f0354689bc1eeb52c505ec01
出典メモuspto-grants-1983_01