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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388796Generated: November 1, 2026

Phenethyl bromide → HCID 3028311, compound

https://huagongshe.com/reaction/1388796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
ReactantEthanone, 1-(2-(4-methylphenyl)-4-quinolinyl)-2-(4-piperidinyl)-HCID 3062071—
SolventDimethylformamideHCID 6228—
ProductHCID 3028311HCID 302831189.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

3.45 g of potassium carbonate and 1.39 g of 2-phenylethyl bromide are added to a solution of 1.72 g of 1-[2-(4-methyl-phenyl)-4-quinolyl]-2-(4-piperidyl)-ethanone, prepared as indicated in Example 8, in 25 ml of dimethylformamide. The suspension, well stirred, is heated for 5 hours at 60° C., then poured into 1 liter of ice-water. The oil which separates is decanted, washed with water, then 100 ml of ether and 100 ml of a 1 N aqueous solution of hydrochloric acid are added. The precipitate formed is filtered, washed with water and then with acetone. 2 g of 1[2-(4-methyl-phenyl)-4-quinolyl]-2-[1-(2-phenyl-ethyl)-4-piperidyl]-ethanone are obtained in the form of dihydrochloride melting at 195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04433150
Source datasetuspto-grants-1984_02
ORD IDord-a156f5e4e22940028b8e95f1cbb49d2a
Source noteuspto-grants-1984_02