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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262217Generated: October 26, 2026

Diethyl Ether → 5-(alpha-Hydroxyundecyl)-3-phenylbenzofuran

https://huagongshe.com/reaction/262217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant5-Bromo-3-phenyl-1-benzofuranHCID 20330164—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-(alpha-Hydroxyundecyl)-3-phenylbenzofuranHCID 21320298—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5.5 g. (0.02 mole) of 5-bromo-3-phenylbenzofuran in tetrahydrofuran is added 0.5 g. (0.02 mole) of magnesium, and the mixture is heated at its reflux temperature for three hours. After cooling to 0° C., 3.4 g. of undecyl aldehyde is added. After stirring for 30 minutes at room temperature, the solution is added to ammonium chloride solution. Evaporation provides a residue which is mixed with diethyl ether and water. The ether layer is separated, washed with saturated sodium chloride solution, dried and evaporated. The resulting oil is dissolved in carbon tetrachloride and eluted from a silica gel column with carbon tetrachloride, then with dichloromethane. The later fractions are evaporated to provide 5-(α-hydroxyundecyl)-3-phenylbenzofuran which is dissolved in dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04153716
Source datasetuspto-grants-1979_05
ORD IDord-c49d250a9e154af5b535095b9dcf3100
Source noteuspto-grants-1979_05