HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 628850Erstellt: 25. Oktober 2026
Dimethylformamide → Methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate
https://huagongshe.com/reaction/628850
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 4-Methoxycarbonylphenylboronic acid | HCID 2734369 | — |
| Edukt | 2-Chloro-6-methoxy-3-methylquinoline | HCID 4914664 | — |
| Katalysator | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate | HCID 66980055 | 25% |
Reaktionsschritte
To a mixture of 2-chloro-6-methoxy-3-methylquinoline (100 mg, 0.482 mmol), 4-(methoxycarbonyl)phenylboronic acid (184 mg, 1.02 mmol), TEA (0.35 mL, 2.41 mmol), and PdCl2(dppf) (35 mg, 0.048 mmol) was added 2 mL of DMF under argon. The mixture was then stirred for 2.5 h at 120° C. in a microwave reactor. The crude mixture was then diluted with water (25 mL) and extracted with EtOAc (25 mL×2). The organics were washed with brine (50 mL), dried over sodium sulfate, and concentrated to yield 250 mg of crude material. The crude was purified via column chromatography with a gradient of 5% EtOAc in hexanes to 80% EtOAc in hexanes to yield 37 mg (25% yield) of methyl 4-(6-methoxy-3-methylquinolin-2-yl)benzoate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09315462B2 |
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| Quelldatensatz | uspto-grants-2016_04 |
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| ORD ID | ord-972b8b97ff7b4039b1d08ea32c45a9ac |
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| Quellennotiz | uspto-grants-2016_04 |
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