HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 545471Erstellt: 23. Oktober 2026
Dimethylformamide dimethyl acetal → Methyl 3-formyl-4-nitrobenzoate
https://huagongshe.com/de/reaction/545471
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Edukt | Methyl 3-methyl-4-nitrobenzoate | HCID 260927 | — |
| Edukt | Sodium periodate | HCID 23667635 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl 3-formyl-4-nitrobenzoate | HCID 10867527 | — |
Reaktionsschritte
A solution of 3-methyl4-nitro-benzoic acid methyl ester (24.99 g, 128.1 mmol) and N,N-dimethylformamide dimethyl acetal (40.0 mL, 300 mmol) was heated at 140° C. for 22.5 h. After cooling to rt, the reaction mixture was concentrated and the residue was crystallized from MeOH to give a purple solid. This solid was dissolved in THF (500 mL) and water (500 mL), and sodium periodate (62.62 g, 292.8 mmol) was added followed by additional sodium periodate (15.6 g, 72.9 mmol) two hours later. After stirring at rt for an additional 1 h, the reaction mixture was filtered through Celite washing with EtOAc (2 L). The filtrate was washed with saturated NaHCO3 (600 mL) and the organic layer was dried over Na2SO4. After filtration, the filtrate was concentrated and the residue was passed through a pad of silica gel, washing with CH2Cl2/hexanes (75%-100%). The filtrate was concentrated and dried to give 3-formyl-4-nitro-benzoic acid methyl ester as yellowish solid. MS (EI): cal'd 210.0 (MH+), exp 210.2 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07935724B2 |
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| Quelldatensatz | uspto-grants-2011_05 |
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| ORD ID | ord-071164a5b10b4466a5f5fec89a3aa0ed |
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| Quellennotiz | uspto-grants-2011_05 |
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