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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486290Generated: October 28, 2026

Potassium Hydroxide → Brofaromine

https://huagongshe.com/reaction/486290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-(7-Bromo-5-methoxy-benzofuran-2-yl)-1-ethoxycarbonyl-piperidineHCID 11143431—
SolventEthylene GlycolHCID 174—
SolventTolueneHCID 1140—
ProductBrofaromineHCID 44571—

Reaction Steps

7.6 g of 4-(7-bromo-5-methoxy-benzofuran-2-yl)-1-ethoxycarbonyl-piperidine are dissolved in 80 ml of ethylene glycol. After the addition of 19.4 g of 86% potassium hydroxide, the resulting cloudy solution is heated at 160° with vigorous stirring for 18 hours. The reaction mixture is cooled to 100°, diluted with 80 ml of toluene, and cooled further to 20°. The reaction solution is extracted twice with 1000 ml of water each time and then four times with 200 ml of a 10% solution of methanesulfonic acid in water each time. The resulting solution in methanesulfonic acid is adjusted to pH 12 by the addition of 30% sodium hydroxide solution and extracted by shaking with 1000 ml of chloroform. The chloroform solution is dried over sodium sulfate, filtered and concentrated by evaporation. Crystallisation from ethyl acetate yields 4-(7-bromo-5-methoxybenzofuran-2-yl)-piperidine having a melting point of 149°-152°. There is obtained from the base by treatment with methanolic hydrochloric acid and recrystallisation from methanol/ether 4-(7-bromo-5-methoxy-benzofuran-2-yl)-piperidine-hydrochloride having a melting point of 242°-243°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290939
Source datasetuspto-grants-1994_03
ORD IDord-2926f403d301454f99ad9142dc4b6a0f
Source noteuspto-grants-1994_03