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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639038Generated: November 3, 2026

Benzyl Bromide → 1-Benzyl-5-butoxypyrrolidin-2-one

https://huagongshe.com/reaction/1639038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 15696557HCID 15696557—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-5-butoxypyrrolidin-2-oneHCID 307796155.6%

Reaction Steps

To a suspension of 4 g of 5-n-butyloxy-pyrrolidin-2-one, 1.79 g of potassium hydroxide hydrated to 85%, and 0.4 g of n-tetrabutylammonium bromide in 80 cm' of tetrahydrofuran, there is added a solution of 4.35 g of benzyl bromide, without exceeding 30° C. After agitating for 1 hour at ambient temperature, the insoluble matter is filtered off and the solvent is evaporated. The residue (4.7 g) is distilled at 230° C. under 0.05 mbar, then the distillate is chromatographed on silica (eluent: ethyl acetate--n-hexane, 1--1). 3.5 g of the expected product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882350
Source datasetuspto-grants-1989_11
ORD IDord-5a0ef2c087df4ed9b59733745d74071d
Source noteuspto-grants-1989_11