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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244008Generated: October 27, 2026

Acetic Acid → 1-(3-Fluoro-2,4-dihydroxy-phenyl)-ethanone

https://huagongshe.com/reaction/2244008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBoron trifluoride etherateHCID 8000—
ReactantBoron tribromideHCID 25134—
Reactant2-Fluoro-3-methoxyphenolHCID 40151763—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(3-Fluoro-2,4-dihydroxy-phenyl)-ethanoneHCID 4512010258%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-fluoro-3-methoxy-phenol (0.5 g, 3.53 mmol) and dichloromethane is stirred at −78° C. A 1M solution of boron tribromide in dichloromethane (3.9 mL, 3.9 mmol) is added slowly and the mixture is stirred 10 min cold, then warmed to 0° C. and stirred 1 hr. The reaction is quenched with ice and stirred at room temperature overnight. The product is extracted with ethyl acetate (2×50 mL), dried over magnesium sulfate, filtered, and concentrated. The resulting residue is combined with boron trifluoride diethyl etherate (1.3 mL, 10.3 mmol) and acetic acid (0.2 mL, 3.28 mmol) and heated to reflux 8 hr. The mixture is cooled to room temperature, diluted with water (50 mL), and extracted with ethyl acetate (3×50 mL). The combined extracts are dried over magnesium sulfate, filtered and concentrated to about 10 mL volume. The resulting mixture is diluted with hexanes (50 mL), cooled to 0° C., and filtered to give the title compound (310 mg, 58%) as a tan solid. MS ES 171 m+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678794B2
Source datasetuspto-grants-2010_03
ORD IDord-7ee900c75fef4f468be035304b253d75
Source noteuspto-grants-2010_03