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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164310Generated: October 25, 2026

Lithium Hydroxide → Aniracetam

https://huagongshe.com/reaction/1164310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantLithium hydrideHCID 62714—
Reactant2-MethoxypyrrolineHCID 12761828—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductAniracetamHCID 2196—

Reaction Conditions

Temperature25 °C

Reaction Steps

276 mg. of lithium hydride (98%), 40 ml. of benzene and 4.2 g. of 2-methoxypyrroline are boiled at reflux for 2 hours under nitrogen and while stirring well. After cooling to 25° C., 6.6 g. of p-methoxybenzoyl chloride dissolved in 25 ml. of benzene are added and the resulting mixture is stirred under reflux for 2 hours and at room temperature for 16 hours. 100 ml. of ethyl acetate followed by 3.0 g. of lithium hydroxide (98%) dissolved in 25 ml. of water are added to the mixture at room temperature within 15 minutes. The organic phase is washed neutral with water, dried over sodium sulfate and evaporated under reduced pressure. After recrystallization from ethanol, there is obtained 1-(p-methoxybenzoyl)-2-pyrrolidinone having a melting point of 119°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04369139
Source datasetuspto-grants-1983_01
ORD IDord-21370e1556bb4704875bf8fa4b26e30f
Source noteuspto-grants-1983_01