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HRID 258339作成日:2026年10月23日

Carbon Dioxide → 2-[p-(Phenoxy)-phenyl]-2-[1-(1H-1,2,4-triazolyl)-methyl]-1,3-dioxolane

https://huagongshe.com/ja/reaction/258339

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物2-[p-(Phenoxycarbonyloxy)-phenyl]-2-[1-(1H-1,2,4-triazolyl)-methyl]-1,3-dioxolaneHCID 19737421—
溶媒Diethyl EtherHCID 3283—
溶媒Ethylene glycol diethyl etherHCID 12375—
生成物2-[p-(Phenoxy)-phenyl]-2-[1-(1H-1,2,4-triazolyl)-methyl]-1,3-dioxolaneHCID 19737389—

反応手順

11 parts of 2-[p-(Phenoxycarbonyloxy)-phenyl]-2-[1-(1H-1,2,4-triazolyl)-methyl]-1,3 -dioxolane are heated in 200 ml ethylene glycol diethyl ether (about 10 hours) at a temperature of 130° C. till the end of the carbon dioxid production. Then the solvent is destilled of under reduced pressure. The oily crude product is cooled to room temperature, solved in 500 ml diethyl ether, washed with two portions of 100 ml water, dried over sodium sulfate and filtered. The solvent is removed by evaporation. The crude product is recrystallised from ethyl acetate/cyclohexane in the presence of active carbon to give colourless crystals with a melting point of 100°-102° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05266585
出典データセットuspto-grants-1993_11
ORD IDord-33c268f57e78493faecfb13e5919d5f1
出典メモuspto-grants-1993_11