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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639039Generated: October 27, 2026

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

https://huagongshe.com/reaction/1639039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Pentyloxy-pyrrolidin-2-oneHCID 15696558—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-5-(pentyloxy)pyrrolidin-2-oneHCID 307796273.8%

Reaction Steps

To a mixture of 4 g of 5-(n-pentyloxy)-pyrrolidin-2-one, 0.4 g of n-tetrabutylammonium bromide and 1.96 g of potassium hydroxide hydrated to 85% in 60 cm3 of tetrahydrofuran, there is added, without exceeding 30° C. a solution of 3.99 g of benzyl bromide in 20 cm3 of tetrahydrofuran. After agitating for 1 hour at ambient temperature, filtering, evaporating to dryness and chromatographing the residue on silica (eluent: ethyl acetate--n-hexane, 1--1), 4.5 g of the expected product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882350
Source datasetuspto-grants-1989_11
ORD IDord-4676a6e415ee4e74aa4a2c70b3b8e8b3
Source noteuspto-grants-1989_11