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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028544Generated: October 28, 2026

2'-Fluoro-4'-methoxyacetophenone → 2-(2-Fluoro-4-methoxyphenyl)-2-propanol

https://huagongshe.com/reaction/1028544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-Fluoro-4'-methoxyacetophenoneHCID 592821—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Fluoro-4-methoxyphenyl)-2-propanolHCID 13493844—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2′-fluoro-4′-methoxyacetophenone (4.45 g, 26.5 mmol) in THF (50 ml) at 0° C., a solution of 2.4 M MeMgBr (11.6 mmol, 27.8 mmol) was added. The mixture was stirred at 0° C. and then room temperature for 4 h. The reaction was quenched with saturated ammonium chloride solution. The organic was extracted with ethyl acetate (3×50 ml). The combined ethyl acetate layers were washed with brine and dried over sodium sulfate. The resulting alcohol was obtained as an oil after flash column using EtOAc:hexane=2:8 as the elute.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735435B2
Source datasetuspto-grants-2014_05
ORD IDord-77634d92baf34aa68cefe50f245a634f
Source noteuspto-grants-2014_05