Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388334Generated: November 1, 2026

Sulfuric Acid → 2-(4-Chlorophenyl)pyrazolidin-3-one

https://huagongshe.com/reaction/1388334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcrylonitrileHCID 7855—
ReactantSodium HydroxideHCID 14798—
ReactantHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Product2-(4-Chlorophenyl)pyrazolidin-3-oneHCID 1327215828.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 4.2 grams (0.05 mole) of sodium bicarbonate in 25 ml of water, 8.9 grams (0.05 mole) of (4-chlorophenyl)hydrazine hydrochloride was added portionwise. After complete addition the mixture was stirred until gas evolution ceased. To this mixture was added 5.5 grams (0.1 mole) of acrylonitrile and the total heated at 80° C. for 4.5 hours. The mixture was cooled and added to a solution of 9.8 grams of concentrated sulfuric acid in 29 ml of water at room temperature. The resultant mixture was heated for one hour at 40° C. and then at reflux for 2.5 hours. This mixture was cooled and added dropwise to a solution of 7.8 grams of sodium hydroxide in 11 ml of water, cooled by an ice bath and stirred for one hour after complete addition. A precipitate formed which was collected by filtration. The filter cake was washed with water, dried under reduced pressure and purified by recrystallization from ethanol to yield 2.78 grams of 2-(4-chlorophenyl)-3-pyrazolidinone (mp 120°-122° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431659
Source datasetuspto-grants-1984_02
ORD IDord-b482905d15ac401da396e1f57903e642
Source noteuspto-grants-1984_02