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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275748Generated: October 26, 2026

Tetrahydrofuran → 3-(2-Chloropyrid 5-yl-methyl)-pyrrolid-2-one

https://huagongshe.com/reaction/275748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Chloro-5-(chloromethyl)pyridineHCID 155479—
ReactantLithium diisopropylamideHCID 2724682—
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 (LDA) in cyclohexane are added dropwise to 31.4 g of N-trimethylsilylpylrolid-2-one in 150 ml of tetrahydrofuran CIF) 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 acetatelhexane (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 numberUS06353001B1
Source datasetuspto-grants-2002_03
ORD IDord-eb0539e64a4e472eb9060b30f3b72282
Source noteuspto-grants-2002_03