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HRID 2198544作成日:2026年10月26日

Phosgene → 2-Chloroformyl-1-phenyl-3-pyrazolidinone

https://huagongshe.com/reaction/2198544

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物PhenidoneHCID 7090—
反応物DiisopropylethylamineHCID 81531—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
溶媒DimethylacetamideHCID 31374—
生成物2-Chloroformyl-1-phenyl-3-pyrazolidinoneHCID 20519578—

反応条件

温度-78 °C

反応手順

To a rapidly mechanically stirred--78° C. solution of dichloromethane (250 ml), containing a 1 N toluene solution of phosgene (204 ml-0.204 mole), and protected by a nitrogen atmosphere, was added a solution of 1-phenyl-3-pyrazolidinone and diisopropylethylamine in 200 ml of a 1:1 mixture of dimethylacetamide (DMA) and dichloromethane [prepared by dissolving 30.0 g(0.185 mole)1-phenyl-3-pyrazolidone in 100 ml of DMA and adding next the dichloromethane and then the diisopropylethylamine (35.5 ml, 0.204 mole]. The addition was rapid but dropwise, requiring≈30 minutes; a precipitate began to appear about 2/3 through the addition. After 10 minutes additional stirring at -78° C., the reaction was quenched by adding 6 ml of concentrated HCl. The reaction was then added to 500 ml of cold 1 N HCL and 500 ml of dichloromethane. After brief shaking the layers were separated and the dichloromethane layer briefly washed with 500 ml of cold 1 N HCl. After drying over anhydrous MgSO4, the solution was concentrated in vacuo to approximately 300 ml and the precipitate which had appeared was collected and washed with ligroin. After drying in vacuo overnight the yield of this white solid was 34.7 g (83%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04358525
出典データセットuspto-grants-1982_11
ORD IDord-b687ebb7bef34d5690c56dd29cf454f8
出典メモuspto-grants-1982_11