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

Temperatur

-78 °C

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%).

1. customprepared
2. additionThe addition
3. additionto appear about 2/3 through the addition
4. customthe reaction was quenched
5. additionby adding 6 ml of concentrated HCl
6. additionThe reaction was then added to 500 ml of cold 1 N HCL and 500 ml of dichloromethane
7. stirringAfter brief shaking the layers
8. customwere separated
9. washthe dichloromethane layer briefly washed with 500 ml of cold 1 N HCl
10. dry with materialAfter drying over anhydrous MgSO4
11. concentrationthe solution was concentrated in vacuo to approximately 300 ml
12. customthe precipitate which had appeared was collected
13. washwashed with ligroin
14. customAfter drying in vacuo overnight the yield of this white solid

ORD-Eintrag

ord-b687ebb7bef34d5690c56dd29cf454f8

Quelldatensatz

uspto-grants-1982_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04358525