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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231559Generated: October 26, 2026

Acetyl chloride → 3-Chloromethyl-1-(4-fluorophenyl)-pyrrolidine-2,5-dione

https://huagongshe.com/reaction/231559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant4-FluoroanilineHCID 9731—
Reactant3-(Chloromethyl)oxolane-2,5-dioneHCID 13592830—
SolventTolueneHCID 1140—
Product3-Chloromethyl-1-(4-fluorophenyl)-pyrrolidine-2,5-dioneHCID 2003347993%

Reaction Conditions

Temperature100 °C

Reaction Steps

In a variant of (b), into a toluene solution of 33.3 g (0.3 moles) 4-fluoroaniline, a toluene solution of 44.6 g (0.3 moles) 2-chloromethylsuccinic acid anhydride were added dropwise at room temperature while stirring. The temperature of the mixture rose to 40° C. during the operation. To the suspension of the semi-anilide obtained, 0.35 moles of acetylchloride was added dropwise at 60° C. while stirring, the addition being carried out so slowly that the ensuing gas development could be easily controlled. After 3 hours the reaction mixture was heated to 100° C. and held at that temperature until the gas development was terminated. The semi-anilide thereby dissolved. When the reaction mixture was cooled down, the desired product crystallized. The actual yield was 93% of the theoretical yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847285
Source datasetuspto-grants-1989_07
ORD IDord-384911e3274b45318b1e9fd76d82376d
Source noteuspto-grants-1989_07