HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 505546Erstellt: 27. Oktober 2026
Potassium Carbonate → 1-Bromo-2,5-dichloro-3-(2-chloro-6-nitrophenoxy)benzene
https://huagongshe.com/reaction/505546
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2,3-Dichloronitrobenzene | HCID 18555 | — |
| Edukt | 3-Bromo-2,5-dichlorophenol | HCID 68428089 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | 1-Bromo-2,5-dichloro-3-(2-chloro-6-nitrophenoxy)benzene | HCID 68425512 | — |
Reaktionsschritte
3-bromo-2,5-dichlorophenol (8.0 g, 33 mmol) and 2,3-dichloronitrobenzene (6.4 g, 33 mmol) were dissolved in NMP (30 mL), followed by the addition of potassium carbonate (5.5 g, 40 mmol). The resulting suspension was placed in an oil bath at 120° C. for 7 hours, after which the reaction mixture was diluted with water (150 mL) and extracted with ethyl acetate (2×00 mL). The combined organic fractions were washed with water (3×100 mL), dried (MgSO4), filtered and the solvent was evaporated under reduced pressure. The resulting residue was purified by column chromatography on silica gel (330 g) eluting with 0-20% CH2Cl2/hexanes to afford the title compound. 1H NMR (CDCl3) δ 7.98 (dd, J=8.2 Hz, J=1.6 Hz, 1H), 7.79 (dd, J=8.2 Hz, J=1.6 Hz, 1H), 7.44 (dd, J=8.2 Hz, J=8.2 Hz, 1H), 7.40 (d, J=2.2 Hz, 1H), 6.54 (d, J=2.2 Hz, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07781454B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-c7fe8dc214444911891a0cee29968636 |
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| Quellennotiz | uspto-grants-2010_08 |
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