Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283143Generated: November 1, 2026

Acetic Acid → 2-(2-Fluoro-4-methoxyphenyl)-2-propanol

https://huagongshe.com/reaction/2283143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
Reactant2'-Fluoro-4'-methoxyacetophenoneHCID 592821—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Fluoro-4-methoxyphenyl)-2-propanolHCID 1349384498%

Reaction Conditions

Temperature30 °C

Reaction Steps

A solution of 2-fluoro-4-methoxyacetophenone (78.1 g, 460 mmol) in tetrahydrofuran (58.6 ml) was added to 3M methylmagnesium chloride solution in THF (199 ml, 598 mmol) at 20 to 35° C. under a nitrogen atmosphere over 30 min without cooling. Additional THF (19.53 ml) was used to rinse all starting material into the vessel. After complete addition, the mixture was stirred at 30° C. for 10 min., then was quenched into acetic acid (52.6 ml, 920 mmol) and water (273 ml) at 5-25° C. THF (20 ml) was used to rinse the vessel. Heptane (156 ml) was then added. The biphasic mixture was stirred at 20-25° C. for 30 min, and then the organic layer was separated. The organic layer was assayed and was found to contain 83.0 g of the desired product, which corresponds to 98% yield. The organic layer was concentrated under vacuum to remove THF, then was flushed with IPAC (200 ml), and the volume was increased to 500 ml by addition of more IPAC. This was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145348B2
Source datasetuspto-grants-2015_09
ORD IDord-8be700fa6cb54655acc79d02c0cc0bb2
Source noteuspto-grants-2015_09