HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24954Erstellt: 25. Oktober 2026
Potassium bisulfate → 3-[1-Methoxy-1-(4-methoxyphenyl)-methylidene]-5-nitro-2-indolinone
https://huagongshe.com/reaction/24954
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium bisulfate | HCID 516920 | — |
| Edukt | 5-Nitroisatin | HCID 4669250 | — |
| Edukt | Diethyl [methoxy(4-methoxyphenyl)methyl]phosphonate | HCID 13262832 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-[1-Methoxy-1-(4-methoxyphenyl)-methylidene]-5-nitro-2-indolinone | HCID 69743130 | — |
Reaktionsschritte
6.3 g (22 mmol) of diethyl [methoxy-(4-methoxyphenyl)-methyl]-phosphonate are dissolved in 40 ml of DMF under a nitrogen atmosphere. 5.1 g (45 mmol) of potassium tert.butoxide are added batchwise at −40° C. and the mixture is then stirred for another 30 minutes at −10° C. Then 3.84 g (20 mmol) of 5-nitroisatine are added. The mixture is stirred for 1 hour at ambient temperature and then poured onto ice water containing 20 ml of saturated potassium hydrogen sulphate solution. The precipitate is suction filtered and chromatographed over silica gel (dichloromethane/methanol=10:1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06855710B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-5dd6cf5d6cb6465cb4268efc2dd2b3be |
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| Quellennotiz | uspto-grants-2005_02 |
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