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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198544Generated: October 25, 2026

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

https://huagongshe.com/reaction/2198544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantPhenidoneHCID 7090—
ReactantDiisopropylethylamineHCID 81531—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventDimethylacetamideHCID 31374—
Product2-Chloroformyl-1-phenyl-3-pyrazolidinoneHCID 20519578—

Reaction Conditions

Temperature-78 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04358525
Source datasetuspto-grants-1982_11
ORD IDord-b687ebb7bef34d5690c56dd29cf454f8
Source noteuspto-grants-1982_11