Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | 3-(Chloromethyl)isoquinoline hydrochloride | HCID 12874871 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3-Ethoxymethylisoquinoline | HCID 12874843 | 88,6% |
Reaktionsschritte
A mixture of 3-chloromethylisoquinoline hydrochloride (40 g) and sodium ethoxide (40 g) in ethanol (700 cc) is heated under reflux for 8 hours. After cooling to 20° C., the mixture is filtered and the filtrate is evaporated to dryness at 50° C. under reduced pressure (20 mm Hg). The residue is taken up in methylene chloride (500 cc), the mixture is washed with water (3×100 cc), the organic phase is dried over magnesium sulphate and filtered and the filtrate is evaporated to dryness at 40° C. under reduced pressure (20 mm Hg). The oily residue is distilled at 110°-114° C. under a pressure of 0.6 mm Hg. 3-Ethoxymethylisoquinoline (31 g), a colourless oil, is obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04261993 |
|---|
| Quelldatensatz | uspto-grants-1981_04 |
|---|
| ORD ID | ord-e1a391845c2d43eeb4c5a2a412c44c74 |
|---|
| Quellennotiz | uspto-grants-1981_04 |
|---|