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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432575Generated: October 24, 2026

1-(Trimethylsilyl)pyrrolidin-2-one → 3-(2-Chloropyrid 5-yl-methyl)-pyrrolid-2-one

https://huagongshe.com/en/reaction/432575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Trimethylsilyl)pyrrolidin-2-oneHCID 84461—
Reactant2-Chloro-5-(chloromethyl)pyridineHCID 155479—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
Product3-(2-Chloropyrid 5-yl-methyl)-pyrrolid-2-oneHCID 18759788—

Reaction Steps

Under a nitrogen atmosphere at a temperature of from −78° C. to −60° C., 180 ml of a 1.5 molar solution of lithium diisopropylamide (IDA) in cyclohexane are added dropwise to 31.4 g of N-trimethylsilylpyrrolid-2-one in 150 ml of tetrahydrofuran (THF) and the reaction mixture is stirred at the same temperature for a further one hour. Then, at from −78° C. to −60° C., 25.5 g of 2-chloro-5-chloromethylpyridine in 40 ml of THF are added, and the mixture is stirred for a further 16 hours at that temperature and then for a further three hours at room temperature. The reaction mixture is poured onto a mixture of ice/water and extracted with ethyl acetate, and the organic phase is separated off The ethyl acetate phase is dried over sodium sulfate and concentrated to dryness by evaporation in vacuo. The residue is purified on silica gel using ethyl acetate/hexane (7:1) as eluant. The title compound having a melting point of 117-118° C. (compound 1.3) is obtained

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664248B2
Source datasetuspto-grants-2003_12
ORD IDord-dec8e6cd826940d6947cf8e1fe93d861
Source noteuspto-grants-2003_12