Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | O-(Dichloromethyl)chlorobenzene | HCID 66624 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Produkt | 2-Chlorobenzaldehyde | HCID 6996 | 97% |
Reaktionsschritte
195.3 g (1.0 mol) of 2-chlorobenza1 chloride are initially charged at 120° C. At this temperature 20 ml (21.8 g, 1.09 mol of water) of a 10% strength aqueous zinc chloride solution are metered in over a period of 5 hours. The mixture is stirred for a further 30 minutes at 120° C. After cooling to room temperature the reaction mixture is extracted with 1×10 ml and 2×5 ml of water. The organic phase is subsequently free of chloride and is worked up by distillation. 136.0 g (97% of theoretical) of 2-chlorobenzaldehyde (b.p.: 90° C./16 torr) with a purity of >99.9% are obtained. The combined aqueous phases (20 ml, 22.0 g) are used in Example 2 as catalyst solution.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05347054 |
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| Quelldatensatz | uspto-grants-1994_09 |
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| ORD ID | ord-65bdd95af8a9428f99b5fa1056b12e76 |
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| Quellennotiz | uspto-grants-1994_09 |
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