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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639042Generated: October 31, 2026

Benzyl Bromide → 1-Benzyl-5-(octyloxy)pyrrolidin-2-one

https://huagongshe.com/reaction/1639042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 15696565HCID 15696565—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-5-(octyloxy)pyrrolidin-2-oneHCID 307796570.5%

Reaction Steps

To a mixture of 2 g of 5-n-octyloxy-pyrrolidin-2-one, 0.65 g of potassium hydroxide at 85% and 0.2 g of tetra-n-butylammonium bromide in 40 cm3 of tetrahydrofuran, there is added a solution of 1.6 g of benzyl bromide in 5 cm3 of tetrahydrofuran, without exceeding 30° C. After agitating for 2 hours at ambient temperature, filtering and evaporating to dryness, the residue is chromatographed on alumina, (eluent: ethyl acetate--cyclo-hexane, 1--1), and 2 g of the expected product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882350
Source datasetuspto-grants-1989_11
ORD IDord-94007ebbc3d94fb99e2ef904bdaa1e76
Source noteuspto-grants-1989_11