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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918992Generated: October 25, 2026

Hydrochloric Acid → 5,5-Dimethyl-3-(3-methylphenyl)pyrrolidine-2,4-dione

https://huagongshe.com/reaction/918992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-BromotolueneHCID 11560—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
Reactant5,5-Dimethylpyrrolidine-2,4-dioneHCID 13346709—
CatalystPalladium ChlorideHCID 24290—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5,5-Dimethyl-3-(3-methylphenyl)pyrrolidine-2,4-dioneHCID 7049623284%

Reaction Conditions

Temperature125 °C

Reaction Steps

Under argon, in a heat-dried apparatus, 1.0 g of solid sodium hydroxide (in the form of so-called “Micropills”) and 15 ml of water- and air-free N-methylpyrrolidone (NMP) are introduced as initial charge. With stirring, 1.907 g of 5,5-dimethylpyrrolidine-2,4-dione are then added and the mixture is stirred for 20 minutes at room temperature. 1.71 g of 3-bromotoluene are then added and the reaction mixture is heated to 125° C. At this temperature, 0.328 g of triphenylphosphine and 89 mg of PdCl2 are then added. The mixture is stirred for 4 hours at 125° C., left to cool to room temperature, stirred into 20 ml of ice-water and adjusted to pH 2 using dilute hydrochloric acid. 20 ml of methylene chloride are added, the mixture is stirred, the phases are separated and the aqueous phase is extracted by shaking two more times with 10 ml of methylene chloride in each case. The combined organic phases are dried and then concentrated on a rotary evaporator. This gives 1.82 g of target product (corresponding to a yield of 84% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09272997B2
Source datasetuspto-grants-2016_03
ORD IDord-3ecb56147d074cf8b1b36318e8850a18
Source noteuspto-grants-2016_03