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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639037Generated: November 2, 2026

Benzyl Bromide → 2-Pyrrolidinone, 5-(1-methylethoxy)-1-(phenylmethyl)-, (+-)-

https://huagongshe.com/reaction/1639037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 15696556HCID 15696556—
SolventTetrahydrofuranHCID 8028—
Product2-Pyrrolidinone, 5-(1-methylethoxy)-1-(phenylmethyl)-, (+-)-HCID 307796071.2%

Reaction Steps

To a suspension of 2.5 g of 5-isopropoxy-pyrrolidin-2-one, 1.23 g of potassium hydroxide hydrated to 85%, and 0.25 g of n-tetra-butylammonium bromide in 50 cm3 of tetrahydrofuran, there is added a solution of 2.99 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 g) is distilled at 200° C. under 0.05 mbar. The distillate is chromatographed on silica (eluent: ethyl acetate--n-hexane, 1--1). 2.9 g of the expected product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882350
Source datasetuspto-grants-1989_11
ORD IDord-3a58b4b7e1d04ec384e52680f8a28cd1
Source noteuspto-grants-1989_11