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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789956Generated: October 30, 2026

Phenol → 4-Chloro-1-(2-hydroxyphenyl)butan-1-one

https://huagongshe.com/reaction/1789956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantBoron trifluoride etherateHCID 8000—
Reactant3-FluorophenolHCID 9743—
Reactant4-Chlorobutyryl chlorideHCID 78370—
Product4-Chloro-1-(2-hydroxyphenyl)butan-1-oneHCID 10867311—
Product4-Chloro-1-(4-fluoro-2-hydroxyphenyl)butan-1-oneHCID 14773873—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a cold boron trifluoride etherate (280 mmol) solution was added 3-fluorophenol or phenol (89 mmol) and 4-chlorobutyryl chloride (178 mmol). The resulting solution was stirred at 130° C. for 18 hours. The reaction mixture was cooled and poured into ice water (100 mL). After stirring for 10 minutes, the water mixture was extracted with ether (3×100 mL). The ether layer was washed with brine (100 mL), dried over MgSO4, filtered and concentrated to a residue to afford 4-chloro-1-(4-fluoro-2-hydroxyphenyl)butan-1-one and 4-chloro-1-(2-hydroxyphenyl)butan-1-one in 52%–67% yield, which was used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071186B2
Source datasetuspto-grants-2006_07
ORD IDord-1904c867b1b84d10aefb06cd7dec1eac
Source noteuspto-grants-2006_07