HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Chloromethyl Methyl Ether → 5-Bromo-3-methoxy-2-(methoxymethoxy)benzaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Chloromethyl Methyl Ether | HCID 7864 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 5-Bromo-2-hydroxy-3-methoxybenzaldehyde | HCID 262238 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-Bromo-3-methoxy-2-(methoxymethoxy)benzaldehyde | HCID 11565322 | 106,8% |
Reaktionsschritte
Ethyldiisopropylamine (3.01 ml, 17.1 mmol) and methoxymethylchloride (1.5 ml, 15.7 mmol) were added to a dichloromethane solution (30 ml) of 5-bromo-2-hydroxy-3-methoxybenzaldehyde (3.3 g, 14.3 mmol) under ice cooling, and the mixture was stirred at room temperature for 2 hours. The reaction solution was washed with water, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1→11:9). The purified product was concentrated to dryness under reduced pressure to obtain 5-bromo-3-methoxy-2-methoxymethoxybenzaldehyde (4.2 g) as light yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08071600B2 |
| Quelldatensatz | uspto-grants-2011_12 |
| ORD ID | ord-6cb00748a0a0469c8784194f0d1e935e |
| Quellennotiz | uspto-grants-2011_12 |