HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1075316Erstellt: 25. Oktober 2026
Potassium Carbonate → Methyl 2-nitro-5-[4-(trifluoromethyl)phenoxy]benzoate
https://huagongshe.com/reaction/1075316
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Edukt | Methyl 5-chloro-2-nitrobenzoate | HCID 171018 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | Methyl 2-nitro-5-[4-(trifluoromethyl)phenoxy]benzoate | HCID 13209694 | 85% |
Reaktionsschritte
p-Hydroxybenzotrifluoride (0.22 g, 1.36 mmol), powdered potassium carbonate (0.185 g, 1.34 mmol), and methyl 5-chloro-2-nitrobenzoate (0.288 g, 1.34 mmol) were heated at 70° C. under a nitrogen atmosphere in 3 ml of dimethyl sulfoxide. After 50 minutes, an aliquot was quenched in methanolic HCl. (By gas chromatography, the reaction is 45% complete.) After 18 hours (overnight), the reaction mixture was cooled to room temperature, diluted with water, and extracted with ether. The organic extracts are shaken with brine, dried (MgSO4) and concentrated to afford methyl 5-(4-trifluoromethylphenoxy)-2-nitrobenzoate in 85% yield. Gas chromatography showed no starting phenol remained. Step B--Methyl 5-(2-chloro-4-trifluoromethylphenoxy) -2-nitrobenzoate
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04395570 |
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| Quelldatensatz | uspto-grants-1983_07 |
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| ORD ID | ord-dce11846ee5d44c2a50ca89293e122f1 |
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| Quellennotiz | uspto-grants-1983_07 |
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