HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48133Erstellt: 24. Oktober 2026
Water → 2-Methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile
https://huagongshe.com/de/reaction/48133
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 2-Hydroxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile | HCID 86759358 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile | HCID 54522751 | 41% |
Reaktionsschritte
2-hydroxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile (1.8 g; 9 mmol) is dissolved in 15 ml of anhydrous tetrahydrofuran, and cooled to 0° C. Methanesulfonyl chloride (0.93 ml, 0.012 mol) is added at once, followed by triethylamine (2 ml, 0.015 mol) dropwise over 20 min, keeping the temperature of the mixture below 5° C. The mixture is then stirred at 2° C. for 1 h 15 min, and poured into 200 ml of iced water. The suspension is extracted with ethyl acetate, the organic extract is washed neutral with water, then with brine, and dried over magnesium sulfate. Rotary evaporation of the solvent and recrystallization from 80 ml of ethanol yields 2-methylsulfonyloxyimino-4-(4-methoxy-phenyl)-but-3-enenitrile (1.02 g; 41%) as light yellow hair-like crystals, mp 147-152° C. (dec). 1H-NMR reveals the presence of only one isomer.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06703182B1 |
|---|
| Quelldatensatz | uspto-grants-2004_03 |
|---|
| ORD ID | ord-212d808d04a24f93b79c9b42fc64dcf5 |
|---|
| Quellennotiz | uspto-grants-2004_03 |
|---|