HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → 2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Ethyl (4-chlorophenyl)acetate | HCID 84177 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | HCID 178483040 | HCID 178483040 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepine | HCID 53941548 | — |
Reaktionsschritte
Add (drop by drop at 90° in a stream of nitrogen to let the alcohol escape) a solution of 4.6 g of sodium in 100 ml of ethyl alcohol to a mixture of 53.2 g of the title compound of Example 1 and 29.8 g of ethyl 4-chlorophenylacetate. Stir it for a further 4 hours at 90° and then cool it to ambient temperature. Mix the cooled reaction mixture with 100 ml of water and 100 ml of diethyl ether, collect the organic phase and dry the latter over sodium sulfate. Concentrate the dried organic phase and then distil off any excess ethyl 4-chlorophenylacetate under a high vacuum to obtain a crude yield [15.5 g (34% of theory)] of the title compound as yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04221788 |
| Quelldatensatz | uspto-grants-1980_09 |
| ORD ID | ord-ca593dee24784df38759aae09bcc0859 |
| Quellennotiz | uspto-grants-1980_09 |