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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618721Generated: October 30, 2026

Hydrochloric Acid → 1-(4-Fluoro-2-methyl-benzofuran-7-yl)-propan-1-ol

https://huagongshe.com/reaction/618721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPropanalHCID 527—
Reactant7-Bromo-4-fluoro-2-methylbenzofuranHCID 21848321—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Fluoro-2-methyl-benzofuran-7-yl)-propan-1-olHCID 2184829168.9%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of 5.75 g (25.1 mmol) of 7-bromo-4-fluoro-2-methylbenzofuran in 90 ml of tetrahydrofuran was added dropwise to a suspension of 0.625 g (27.5 mmol) of Mg in 100 ml of boiling tetrahydrofuran and the mixture was stirred at reflux for 2.5 hours. Subsequently, it was cooled to 10° C., 2.75 ml (37.5 mmol) of propionaldehyde were added dropwise thereto and the mixture was stirred for 30 minutes. The mixture was poured into 200 ml of 1N hydrochloric acid and extracted three times with 150 ml of dichloromethane. After drying over sodium sulfate concentration was carried out in a vacuum. The crude product obtained was purified by column chromatography on silica gel (dichloro-methane/hexane 4:1). 3.6 g (55%) of 1-(4-fluoro-2-methyl-benzofuran-7-yl)-propan-1-ol were obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05955495
Source datasetuspto-grants-1999_09
ORD IDord-f36c733d391b4cd5a621cfbefcd38de5
Source noteuspto-grants-1999_09