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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700626Generated: November 2, 2026

Phosphorus trichloride → 2',5-Dichloro-1,6-dihydro[1,1'-biphenyl]-3(2H)-one

https://huagongshe.com/reaction/1700626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus trichlorideHCID 24387—
Reactant5-(2-Chlorophenyl)cyclohexane-1,3-dioneHCID 875360—
SolventChloroformHCID 6212—
Product2',5-Dichloro-1,6-dihydro[1,1'-biphenyl]-3(2H)-oneHCID 18317399—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-(2-chlorophenyl)cyclohexane-1,3-dione (3.0 g) in chloroform(10 ml) was added phosphorus trichloride (0.62 g), and the mixture was stirred at 100° C. for 2.5 hours. To the mixture was added phosphorus trichloride (0.62 g), and the mixture was stirred at 100° C. for 2 hours. The reaction solution was concentrated under reduced pressure, and to the residue was added ice-water. The mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure to give 3-chloro-5-(2-chlorophenyl)-2-cyclohexen-1-one, which was dissolved in ethanol (3 ml). To the solution were added sodium sulfide 9 hydrate (2.0 g) and water (3 ml), and the mixture was stirred at room temperature for 2 hours and concentrated under reduced pressure. The residue was dissolved in water, and the solution was washed with diethylether. To the aqueous layer was added 4N hydrochloric acid to make the solution acidic, and the solution was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure to give oil of 5-(2-chlorophenyl)-3-mercapto-2-cyclohexen-1-one (1.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-cb67c95dea8f4de6b2bdd38e795dc811
Source noteuspto-grants-2002_02