Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587004Generated: November 2, 2026

Phenethyl bromide → 5,6,7,8-tetrahydro-5-oxo-1-(2-phenylethyl)-2(1H)-quinolinone

https://huagongshe.com/reaction/1587004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantLithium hydrideHCID 62714—
Reactant2-Hydroxy-7,8-dihydro-5(6H)-quinolinoneHCID 267450—
SolventDimethylformamideHCID 6228—
Product5,6,7,8-tetrahydro-5-oxo-1-(2-phenylethyl)-2(1H)-quinolinoneHCID 1035561824.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 5,6,7,8-tetrahydro-5-oxo-2(1H)-quinolinone (7.5 g), lithium hydride (0.59 g), and dimethylformamide (300 ml) was stirred for 3 hrs at 25° C., under nitrogen. 2-Phenylethyl bromide (9.36 g) was added and the mixture was stirred for an additional eighteen hrs. The reaction mixture was concentrated and the residue was partitioned between ethyl acetate and water. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was triturated with petroleum ether to afford 3.0 g (24%) of 5,6,7,8-tetrahydro-5-oxo-1-(2-phenylethyl)-2(1H)-quinolinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05216164
Source datasetuspto-grants-1993_06
ORD IDord-e2c608bcfff943f982e911bd9ee02a86
Source noteuspto-grants-1993_06