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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965982Generated: October 30, 2026

Acetyl chloride → 2'-Fluoro-4'-hydroxyacetophenone

https://huagongshe.com/reaction/965982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant3-FluorophenolHCID 9743—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
Product2'-Fluoro-4'-hydroxyacetophenoneHCID 27249128.4%

Reaction Steps

To a stirred suspension of aluminum chloride (42 g, 312 mmol) in 1,2-dichloroethane (100 ml) was added 3-fluorophenol (31 g, 276 mmol) dropwise at 0° C. After addition acetyl chloride (24 g, 306 mmol) was added dropwise and then the mixture was heated at reflux temperature for 16 hours. The mixture was cooled down to room temperature, and poured into ice. The whole was extracted with diethylether. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was recystallized with hexane to give title compound (3.57 g, 8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951876B2
Source datasetuspto-grants-2005_10
ORD IDord-41cb10f67815463b8b0424a8190c81e1
Source noteuspto-grants-2005_10