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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56304Generated: October 30, 2026

Hydrochloric Acid → 1-(4-Chloro-3-fluorophenyl)propan-2-one

https://huagongshe.com/reaction/56304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetylacetoneHCID 31261—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Bromo-1-chloro-2-fluorobenzeneHCID 2724690—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product1-(4-Chloro-3-fluorophenyl)propan-2-oneHCID 1104147348.3%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a mixture of 4-bromo-1-chloro-2-fluorobenzene (20.90 g, 100.0 mmol) and acetylacetone (30 mL, 300.0 mmol) in DMSO (100 mL) were added tripotassium phosphate (63.70 g, 300.0 mmol) and CuI (3.00 g, 15.80 mmol) under N2 and the mixture was stirred at 110° C. for 23 h. The mixture was cooled to rt and hydrochloric acid (300 mL, 2 M) was added. The resulting mixture was extracted with EtOAc (100 mL×3) and the combined organic phases were washed with brine (100 mL×2), dried over anhydrous Na2SO4 (50 g), and filtered. The filtrate was concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=10:1) to give the title compound as yellow liquid (9.02 g, 48.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434695B2
Source datasetuspto-grants-2016_09
ORD IDord-91ce1cfa23d94c04826d62bc2656608b
Source noteuspto-grants-2016_09