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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582756Generated: November 1, 2026

2-(2-Acetoxy-4-fluorophenoxy)ethanol → 2-(2-Hydroxy-4-fluorophenoxy)ethanol

https://huagongshe.com/reaction/1582756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Acetoxy-4-fluorophenoxy)ethanolHCID 22718367—
ReactantHCID 86597229HCID 86597229—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Hydroxy-4-fluorophenoxy)ethanolHCID 22718235—

Reaction Conditions

Temperature90 °C

Reaction Steps

2-(2-Acetoxy-4-fluorophenoxy)ethanol 1.53 g was dissolved in a mixed solvent of tetrahydrofuran 10 ml and water 5 ml, then lithium hydroxide monohydride 294 mg was added thereto, and the mixture was stirred at 90° C. After stirred for 10 hours, the reaction mixture was cooled and partitioned by adding water and ethyl acetate. The organic layer was washed with water and then with brine, dried over magnesium sulfate anhydride and evaporated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate system), whereby the title compound (1.07 g, 80%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737425B1
Source datasetuspto-grants-2004_05
ORD IDord-12524f5734e5433b93ec789952030b17
Source noteuspto-grants-2004_05