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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198611Generated: October 31, 2026

Tetrahydrofuran → 107259-16-5

https://huagongshe.com/reaction/1198611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15223491HCID 15223491—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
Product107259-16-5HCID 19000545—

Reaction Steps

Lithium aluminum hydride (0.55 g, 0.014 mole) was added to tetrahydrofuran (45 mL) with stirring under nitrogen. 4-(1-Aminoethyl)-1-benzyl-2-oxopyrrolidine (1.60 g, 0.0073 mole) was added in several portions over 30 minutes and the reaction was brought to reflux over 75 minutes. The reaction was refluxed 16 hours and cooled to room temperature. The reaction was treated with water (0.55 mL), 10% NaOH (0.55 mL), and water (1.65 mL) slowly dropwise and the solid filtered off and washed with dichloromethane. The combined filtrates were evaporated under reduced pressure to give 3-(1-aminoethyl)-1-benzylpyrrolidine isomer A (1.05 g, 70%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281612
Source datasetuspto-grants-1994_01
ORD IDord-62c41d28f80d410ca03713b31cb8b067
Source noteuspto-grants-1994_01