HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23820Erstellt: 24. Oktober 2026
Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)- → 2,5-Dichloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamide
https://huagongshe.com/de/reaction/23820
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)- | HCID 11037 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | Hydrochloride methanol | HCID 21893726 | — |
| Edukt | 2,5-dichloro-N-(2-hydroxyimino-ethyl)-benzamide | HCID 73987900 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 2,5-Dichloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamide | HCID 22590612 | 40% |
Reaktionsschritte
To a solution of 2,5-dichloro-N-(2-hydroxyimino-ethyl)-benzamide (0.72 g, 2.9 mmol) in MeOH (20 mL) under an argon atmosphere at 0° C. was added methyl orange (trace) followed by a saturated solution of MeOH/HCl until a persistent red color was observed. Sodium cyanoborohydride (0.22 g, 3.5 mmol) was dissolved in MeOH (5 mL) and was added sequentially with saturated MeOH/HCl over 0.5 h. The reaction mixture was stirred an additional 1 h and the MeOH was removed in vacuo. The residue was basidified with saturated Na2CO3 and extracted (7×25 mL) with dichloromethane/MeOH (9:1). The combined organic extracts were washed with brine, were dried (Na2SO4) and were concentrated. The residue was purified by flash chromatography (2%-5% MeOH/dichloromethane) to provide the title compound (0.29 g, 40%) as a white solid. 1H NMR (400 MHz, CD3OD): δ 7.53 (s, 1H); 7.44 (s, 2H); 3.56 (t, j=6.2 Hz, 2H); 3.06 (t, j=6.2 Hz, 2H). ESMS: M+H=249.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06852882B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-82447eab617b430281efa9b577a3071a |
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| Quellennotiz | uspto-grants-2005_02 |
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