HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 577461Erstellt: 26. Oktober 2026
Potassium Persulfate → HCID 21907510, Verbindung
https://huagongshe.com/reaction/577461
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Persulfate | HCID 24412 | — |
| Edukt | Methyl 3-Bromo-2-methylbenzoate | HCID 12929135 | — |
| Katalysator | Dichloro(p-cymene)ruthenium(II) dimer | HCID 10908223 | — |
| Lösungsmittel | Trifluoroacetic acid | HCID 6422 | — |
| Lösungsmittel | Trifluoroacetic anhydride | HCID 9845 | — |
| Produkt | HCID 21907510 | HCID 21907510 | 75,4% |
Reaktionsschritte
A solution of methyl 3-bromo-2-methylbenzoate (Cpd FF, 2.40 g, 10.5 mmol) in trifluoroacetic acid (50 mL) and trifluoroacetic anhydride (20 mL) in a sealed tube was treated with potassium persulfate (3.12 g, 11.5 mmol) and dichloro(p-cymene)ruthenium(II) dimer (0.170 g, 0.278 mmol). The reaction mixture was heated at 85° C. overnight. The volatiles were removed under vacuum and the resulting residue was taken up in dichloromethane and water. The aqueous phase was brought to pH˜5 with K3PO4 (sat. aq.). The layers were separated and the organic layer purified by column chromatography (0-30% ethyl acetate/heptane) to give methyl 3-bromo-6-hydroxy-2-methylbenzoate (Cpd GG, 1.94 g, 75%) as a clear oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09040515B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-3b8b36d332aa42ca8a818bc02619cecf |
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| Quellennotiz | uspto-grants-2015_05 |
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