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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023850Generated: October 31, 2026

Water → 1-(5-Chloro-4-fluoro-2-hydroxyphenyl)ethanone

https://huagongshe.com/reaction/1023850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuryl chlorideHCID 24648—
Reactant4'-Fluoro-2'-hydroxyacetophenoneHCID 2737326—
SolventAcetic AcidHCID 176—
Product1-(5-Chloro-4-fluoro-2-hydroxyphenyl)ethanoneHCID 16221436—
Product1-(3-Chloro-4-fluoro-2-hydroxyphenyl)ethan-1-oneHCID 67205236—

Reaction Conditions

Temperature120 °C

Reaction Steps

To 1-(4-fluoro-2-hydroxyphenyl)ethanone (1.7 g, 11.03 mmol) in glacial acetic acid (24 mL) at 10° C. was slowly added sulfuryl chloride (2.23 g, 16.54 mmol). The mixture was heated to 120° C. and was allowed to stir for overnight. The solution was cooled down to room temperature and poured into water (30 mL). The water layer was extracted with EtOAc for three times. The EtOAc was washed with satd. Aq NaHCO3, water, brine, dried (Na2SO4) and concentrated recrystallized The mix was purified by column chromatography using 1:10 Hexanes:Ethyl acetate to yield 234 mg of 1-(5-chloro-4-fluoro-2-hydroxyphenyl)ethanone and 400 mg of 1-(3-chloro-4-fluoro-2-hydroxyphenyl)ethanone. These compounds were used in the next step without characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722720B2
Source datasetuspto-grants-2014_05
ORD IDord-291ab45ed0594c0eb9c6f024e2e881dc
Source noteuspto-grants-2014_05