Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604594Generated: October 25, 2026

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

https://huagongshe.com/reaction/604594

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-Fluoro-4'-methoxyacetophenoneHCID 592821—
ReactantHCID 178418573HCID 178418573—
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 dry THF (50 mL) at 0° C., a solution of 2.4 M methyl magnesium bromide (11.6 mL, 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 NH4Cl solution. The organic was extracted with EtOAc (3×50 mL). The combined EtOAc layers were washed with brine and dried over Na2SO4. The resulting alcohol was obtained as an oil after flash chromatography using EtOAc:hexane=2:8 as the eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-9a1bb05199f54be2b7b7cd02a6f352ce
Source noteuspto-grants-2011_03