HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505519Generated: October 26, 2026
Potassium Carbonate → 2-(3-Bromo-5-chlorophenoxy)-1-chloro-3-nitrobenzene
https://huagongshe.com/reaction/505519
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Dichloronitrobenzene | HCID 18555 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Bromo-5-chlorophenol | HCID 22630180 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-(3-Bromo-5-chlorophenoxy)-1-chloro-3-nitrobenzene | HCID 56833647 | — |
Reaction Steps
2,3-dichloronitrobenzene (764 mg, 3.99 mmol), 3-bromo-5-chlorophenol (1.65 g, 7.98 mmol) and potassium carbonate (661 mg, 4.79 mmol) were suspended in NMP (5 mL) and placed in an oil bath at 120° C. After 2 hours, the reaction was allowed to cool to room temperature, saturated aqueous ammonium chloride (10 mL) was added and the mixture was extracted with ethyl acetate (2×50 mL). The combined organic fractions were washed with dilute brine (4×50 mL), dried (MgSO4), filtered and the solvent was evaporated under reduced pressure. The residue was purified by automated column chromatography on silica gel (80 g), eluting with 0-100% CH2Cl2/hexanes to yield the title compound. 1H NMR (CD3CN) δ 8.02 (dd, J=8.3 Hz, J=1.5 Hz, 1H), 7.88 (dd, J=8.2 Hz, J=1.6 Hz, 1H), 7.52 (dd, J=8.2 Hz, J=8.3 Hz, 1H), 7.38 (m, 1H), 7.07 (m, 1H), 6.97 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781454B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-87d3c660e6a54c859f4fba2caddc8efa |
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| Source note | uspto-grants-2010_08 |
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