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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637686Generated: October 30, 2026

1,4-Dibromobutane → 5-Chloro-3-methyl-6-(pyrrolidin-1-yl)-benzofuran

https://huagongshe.com/reaction/637686

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Amino-5-chloro-3-methylbenzofuranHCID 20255647—
SolventEthanolHCID 702—
Product5-Chloro-3-methyl-6-(pyrrolidin-1-yl)-benzofuranHCID 20255649—

Reaction Steps

A mixture of 9.1 g (50 mmole) of 6-amino-5-chloro-3-methylbenzofuran, 11.8 ml (0.1 mole) of 1,4-dibromobutane, 17.1 ml (0.1 mole) of N-ethyldiisopropylamine and 60 ml of ethanol is boiled under reflux for 24 hours and then concentrated by evaporation in vacuo. The residue is partitioned between methylene chloride and saturated sodium bicarbonate solution. The crude product obtained after drying and concentration by evaporation of the methylene chloride is chromatographed with petroleum ether/ether over silica gel. Subsequent distillation in a bulb tube (150°/10-1 torr) yields 5-chloro-3-methyl-6-(pyrrolidin-1-yl)-benzofuran having a melting point of 50°-52°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04558043
Source datasetuspto-grants-1985_12
ORD IDord-220f058344494205a4cde4decc2594ca
Source noteuspto-grants-1985_12