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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380326Generated: October 31, 2026

Phenethyl bromide → HCID 13536280, compound

https://huagongshe.com/reaction/1380326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13752627HCID 13752627—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 13536280HCID 13536280—

Reaction Steps

To a solution of 0.6 g of 5-fluoro-N-(4-piperidyl)indole-3-carboxamide in a mixture of 50 ml of toluene and 10 ml of dimethylformamide were added 0.43 g of 2-phenylethylbromide and 1 g of potassium carbonate, and the whole mixture was stirred while heating and refluxing for 7 hours. After cooling, to the reaction mixture was added 50 ml of ice-cold water and stirred for 1 hour. The precipitated crystals were filtered, and washed with water and ethyl acetate. An organic layer was separated from the filtrate, dried over magnesium sufate and concentrated under reduced pressure. The residue was treated with a small amount of ethyl acetate to crystallize, and the crystals were filtered and combined with the crystals obtained as above. All of the crystals were recrystallized from methanol to give 5-fluoro-N-[1-(2-phenylethyl)-4-piperidyl]indole-3-carboxamide, melting at 238°-240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581355
Source datasetuspto-grants-1986_04
ORD IDord-b77d4e393e1e4bc4915c878819495dcf
Source noteuspto-grants-1986_04