HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607318Generated: November 3, 2026
Hydrochloric Acid → 4-(4-Bromo-2-nitro-phenylsulfanyl)-phenol
https://huagongshe.com/reaction/607318
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Mercaptophenol | HCID 240147 | — |
| Reactant | 4-Bromo-1-fluoro-2-nitrobenzene | HCID 2736328 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Bromo-2-nitro-phenylsulfanyl)-phenol | HCID 61031468 | 107.3% |
Reaction Steps
A mixture of 4-bromo-1-fluoro-2-nitrobenzene (0.44 g, 2.0 mmol), 4-mercaptophenol (0.303 g, 2.4 mmol), and cesium carbonate (1.56 g, 4.8 mmol, 2.4 eq) in dimethylformamide (10 mL) was heated in a 100° C. oil bath for 3 hours and then cooled to room temperature. The reaction mixture was poured over ice water (50 mL), adjusted to pH 3 by the addition of 1N aqueous hydrochloric acid, and extracted with ethyl acetate (3×100 mL). The combined organic layers were dried over anhydrous magnesium sulfate, filtered and evaporated to provide the title compound as a thick yellow oil (0.70 g, >100%) that was utilized without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915411B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-b69b8634fde74362bc0872748a4c1f82 |
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| Source note | uspto-grants-2011_03 |
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