HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 422721Erstellt: 24. Oktober 2026
Benzene, 4-chloro-1-methyl-2-nitro- → 4-Chloro-2-nitrobenzaldehyde
https://huagongshe.com/de/reaction/422721
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzene, 4-chloro-1-methyl-2-nitro- | HCID 6975 | — |
| Edukt | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Chloro-2-nitrobenzaldehyde | HCID 79674 | — |
Reaktionsschritte
A solution of 4-chloro-2-nitrotoluene (514.8 mg, 3.000 mmol) and dimethylformamide dimethylacetal (1.200 ml, 1074 mg, 9.000 mmol) in DMF (1.2 ml) was heated at 135° C. in a sealed tube for 15 h. The reaction mixture was cooled to rt and added dropwise to a 20° C. solution of NaIO4 (1926 mg, 9.000 mmol) in water (6.18 ml) and DMF (3.09 ml). After 3 h, the mixture was treated with water (20 ml) and extracted with EtOAc (3×15 ml). The extracts were washed with water (3×15 ml) and brine (15 ml), and dried over MgSO4. After the solid was filtered off and the solvent was removed in vacuo, a brown solid of 4-chloro-2-nitrobenzaldehyde was obtained (J. Org. Chem. 2003, 68, 4104-4107). 1H NMR (CDCl3, 400 MHz) δ 7.74-7.78 (m, 1H), 7.94-7.96 (m, 1H), 8.11-8.12 (m, 1H), 10.39 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08101613B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-5250471e55c04dd19b4a344b49656d9f |
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| Quellennotiz | uspto-grants-2012_01 |
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