戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 893954作成日:2026年10月27日

Methane → 1-(N-Chloroacetyl-carbamoyl)-2-cyanoaziridine

https://huagongshe.com/reaction/893954

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物TolueneHCID 1140—
反応物Chloroacetyl isocyanateHCID 78209—
反応物Aziridine-2-carbonitrileHCID 118115—
溶媒Ethyl AcetateHCID 8857—
生成物1-(N-Chloroacetyl-carbamoyl)-2-cyanoaziridineHCID 21161941—

反応手順

A solution of 36 g. chloroacetyl isocyanate in 100 ml. toluene is added dropwise, while stirring and cooling, at a temperature of 20° to 30° C. to 20.4 g. 2-cyanoaziridine dissolved in 200 ml. toluene. The resulting suspension is further stirred for 1 hour at ambient temperature, then filtered with suction. The solid material obtained is washed with toluene and triturated with diethyl ether to give 62 g. of crude product. This is introduced into about 2.5 to 3 liters ethyl acetate at a temperature of 60° C., boiled for a short time and the clear solution treated with active charcoal. After filtration, the clear and still hot filtrate is evaporated in a vacuum and the evaporation residue is triturated with anhydrous diethyl ether and dried for 1 hour at 70° C. There are obtained 39.3 g. of product with a melting point of 152°-155° C. After further purification by stirring for 5 minutes with 200 ml. ethyl acetate at 60° C. and trituration of the crystals obtained with diethyl ether, there are obtained, after drying in a vacuum at 70° C. 28.9 g. 1-(N-chloroacetyl-carbamoyl)-2-cyanoaziridine; m.p. 152°-155° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04282212
出典データセットuspto-grants-1981_08
ORD IDord-95d1922f260b4e2488e5cae8440755bc
出典メモuspto-grants-1981_08