Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromine | HCID 24408 | — |
| Edukt | 2-Hydroxy-4-Methoxybenzaldehyde | HCID 69600 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-Bromo-2-hydroxy-4-methoxybenzaldehyde | HCID 818108 | 80% |
Reaktionsschritte
Ex-13B: 2-Hydroxy-4-methoxybenzaldehyde (6.0 g, 39 mmol) was dissolved in dichloromethane (50 mL) and cooled to 0° C. using an ice-water bath. Bromine (6.8 g, 43 mmol) in dichloromethane (2 mL) was added dropwise to the cooled solution and stirred for 2 h at 0° C. The mixture was warmed to room temperature and stirred for an additional 1 h and the resulting yellow precipitate was collected. Recrystallization (ethyl acetate/hexanes) yielded 7.1 g (80%) of 5-bromo-2-hydroxy-4-methoxybenzaldehyde as white needles, mp 63–64° C. 1H-NMR (300 MHz, CDCl3) δ 11.43 (s, 1H), 9.69 (s, 1H), 7.68 (s, 1H), 6.48 (s, 1H), 3.95 (s, 3H). Anal. Calcd. for C8H7BrO3: C, 41.59; H, 3.05; Found: C, 41.86; H, 3.05.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07173129B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-962d1f5d4d6e4c1a8c20f5a49f95f37b |
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| Quellennotiz | uspto-grants-2007_02 |
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