HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6897Erstellt: 24. Oktober 2026
Methane, dichloromethoxy- → 2-Fluoro-4,5-dimethoxybenzaldehyde
https://huagongshe.com/de/reaction/6897
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methane, dichloromethoxy- | HCID 21004 | — |
| Edukt | 4-Fluoro-1,2-dimethoxybenzene | HCID 593640 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Fluoro-4,5-dimethoxybenzaldehyde | HCID 603595 | — |
Reaktionsschritte
In a flame-dried, round-bottomed flask fitted with a magnetic stirrer and N2 inlet was placed 4-fluoroveratrole (0.78 g, 5.0 mmol, Aldrich Chemical Co.) in 20 ml of anhydrous CH2Cl2. After cooling to 0° C., titanium (IV) chloride (0.91 ml, 1.57 g, 8.3 mmol) was added, followed after 10 min. by a,a-dichloromethyl methyl ether (0.45 ml, 0.575 g, 5.0 mmol). The mixture was allowed to warm to room temperature and after 2 hr it was quenched with an excess of aqueous saturated NaHCO3. The suspension was filtered through a pad of d.e. (diatomaceous earth), the aqueous phase was extracted with additional amounts of CH2Cl2 and the organic phases were combined and washed with water followed by saturated aqueous NaCl. After drying with MgSO4, the organic solvent was removed in vacuo to give the title compound as a white solid, 910 mg.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07084165B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-cea5963e61c54fcea99b57a43cf1be79 |
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| Quellennotiz | uspto-grants-2006_08 |
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