Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639036Generated: November 3, 2026

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

https://huagongshe.com/reaction/1639036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 15696555HCID 15696555—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-5-propoxypyrrolidin-2-oneHCID 307795961.4%

Reaction Steps

To a mixture of 4 g of 5-(n-propyloxy)-pyrrolidin-2-one, 0.4 g of n-tetrabutylammonium bromide and 2.34 g of potassium hydroxide hydrated to 85% in 70 cm3 of tetrahydrofuran, there is added a solution of 4.78 g of benzyl bromide in 25 cm3 of tetrahydrofuran, operating at between 20° C. and 30° C. After agitating for 1 hour, filtering and then evaporating under reduced pressure, the residue is chromatographed on silica, (eluent: ethyl acetate--n-hexane, 1--1). 4 g of the expected product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882350
Source datasetuspto-grants-1989_11
ORD IDord-452bdca9e98a4fd3ae222ca194617d99
Source noteuspto-grants-1989_11