HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707648Generated: October 31, 2026
2,5-Dichloronitrobenzene → 4-Chloro-2-nitro-1-(phenylthio)benzene
https://huagongshe.com/reaction/1707648
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Dichloronitrobenzene | HCID 6977 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-2-nitro-1-(phenylthio)benzene | HCID 376977 | 57% |
Reaction Steps
Potassium hydroxide (6.15 g; 87%) was added to a stirred solution of thiophenol (10.0 g) in N,N-dimethylformamide (170 mL) at room temperature. When most of the potassium hydroxide appeared to have dissolved, 2,5-dichloronitrobenzene (17.4 g) was added, and the initially dark solution turned bright yellow with some precipitate. The reaction was placed in an oil bath at 70° C. for three hours, and then evaporated in vacuo. The residue was partitioned between chloroform and 1N NaOH and the layers were separated. The aqueous layer was extracted once more with chloroform. The chloroform solutions were combined, washed with 1N NaOH, H2O, 1N HCl, H2O and brine, dried over MgSO4, and evaporated in vacuo. The resulting oil was treated with cyclohexane, and the product crystallized. The crystalline product was collected by filtration, washed with hexane, and dried in vacuo at 56° C. to yield 13.73 g (57%) of yellow crystals. mp: 84°-86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05354747 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-cac4e7e4df02489c9e164571b1805025 |
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| Source note | uspto-grants-1994_10 |
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