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HRID 5749作成日:2026年10月24日

Carbon Dioxide → Diethyl Pyrocarbonate

https://huagongshe.com/ja/reaction/5749

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Ethyl chloroformateHCID 10928—
反応物Carbonate IonHCID 19660—
反応物Sodium ethoxideHCID 2723922—
反応物SodiumHCID 5360545—
反応物PyrocarbonateHCID 15238643—
反応物Sodium ethyl carbonateHCID 23677505—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物Diethyl PyrocarbonateHCID 3051—
生成物Sodium ChlorideHCID 5234—

反応手順

The organic pyrocarbonates may be prepared by reacting alkali metal organic carbonate, e.g., sodium ethyl carbonate, with organic halocarbonate, e.g., ethyl chlorocarbonate (ethyl chloroformate). The organo groups of the organic carbonate and halocarbonate are chosen to correspond to the organo groups desired for the pyrocarbonate. For example, sodium ethoxide, which can be prepared by dissolving sodium metal in a toluene solution of ethyl alcohol, is carbonated with carbon dioxide to prepare sodium ethyl carbonate. Thereafter, the sodium ethyl carbonate is reacted with ethyl chloroformate to form diethyl pyrocarbonate and sodium chloride. The chloride salt is filtered and the pyrocarbonate recovered by distillation.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246630
出典データセットuspto-grants-1993_09
ORD IDord-c92cfeae8c76411db9a7c282c6b1f728
出典メモuspto-grants-1993_09