HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1893143Erstellt: 27. Oktober 2026
8-Methoxyquinoline → 8-Methoxy-2-(2-methoxyphenyl)quinoline
https://huagongshe.com/reaction/1893143
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 8-Methoxyquinoline | HCID 70310 | — |
| Edukt | Ethyl acetate hexane | HCID 21226206 | — |
| Edukt | HCID 178506687 | HCID 178506687 | — |
| Katalysator | HCID 178418406 | HCID 178418406 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 8-Methoxy-2-(2-methoxyphenyl)quinoline | HCID 67256584 | — |
Reaktionsschritte
A solution of 8-methoxyquinoline (5.54 g, 34.8 mmol, 1.0 eq) in 55 ml diethyl ether was slowly dropped (within about 30 min) into a solution of o-lithioanisole (4.37 g, 38.4 mmol, 1.1 eq) in 55 ml diethyl ether (each 55 mL). A yellow green fluorescing solution was formed. At the conclusion of the addition, stirring was continued at room temperature for a further 2 hours, after which no more educt could be detected by thin layer chromatography. During the reaction, the color of the reaction mixture changed from fluorescent yellow to green to green-brown. The reaction mixture was worked up by adding it to ice and subsequent extraction with diethyl ether (3×40 ml). The combined organic phases (yellow) were dried over MgSO4 and the solvent was removed in a rotary evaporator. The residue was dissolved in 200 ml dichloromethane and stirred with ca. 40 equivalents of activated manganese dioxide (Merck) until the thin layer chromatographic control (ethyl acetate/hexane=4/6) showed that all of the crude product had reacted. The manganese dioxide was filtered off and the solvent removed in the rotary evaporator. The product was dried under vacuum.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08513177B2 |
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| Quelldatensatz | uspto-grants-2013_08 |
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| ORD ID | ord-14b7c19316fd4cf2abc8f9176a91023f |
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| Quellennotiz | uspto-grants-2013_08 |
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