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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | 5-(2-Chlorophenyl)cyclohexane-1,3-dione | HCID 875360 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2',5-Dichloro-1,6-dihydro[1,1'-biphenyl]-3(2H)-one | HCID 18317399 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350749B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-cb67c95dea8f4de6b2bdd38e795dc811 |
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| Source note | uspto-grants-2002_02 |
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