HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Thionyl Chloride → HCID 178438090, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | Propionamidine hydrochloride | HCID 415117 | — |
| Edukt | Hydroxyamine hydrochloride | HCID 443297 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Oxathiadiazolone | HCID 22315334 | — |
| Edukt | N'-hydroxy-2-(naphthalen-2-yl)propanimidamide | HCID 53747220 | — |
| Produkt | HCID 178438090 | HCID 178438090 | — |
Reaktionsschritte
The monomethyl compound (5.07 g) was converted to the N'-hydroxy-2-(naphthalen-2-yl)propanimidamide following the procedure of Example 1, with hydroxylamine hydrochloride and sodium ethoxide at reflux for three days. The product (4.18 g) was converted to the oxathiadiazole-2-oxide following the procedure of Example 1. The addition of thionyl chloride to the propanimidamide was performed at 0° C. over a thirty minute period. The crude product was purified by flash chromatography through a silica gel column employing dichloromethane, 0.5% ethyl acetate/dichloromethane, 1% ethyl acetate and 2% ethyl acetate serial elution solvents. The product is a light yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04910019 |
| Quelldatensatz | uspto-grants-1990_03 |
| ORD ID | ord-5fecb679a9c849cda2bb8de44c7ea071 |
| Quellennotiz | uspto-grants-1990_03 |