HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydroquinone → Chloroadamantylidene adamantane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydroquinone | HCID 785 | — |
| Edukt | Chlorosuccinimide | HCID 31398 | — |
| Edukt | Biadamantylidene | HCID 141567 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Chloroadamantylidene adamantane | HCID 12950367 | — |
Reaktionsschritte
To a solution of 1 mmol (268 mg) adamantylidene adamantane having the formula 19 in 20 cm3CH2Cl2, 1.05 mmoles (140 mg) N-chlorosuccinimide was added. The reaction mixture was stirred at room temperature for 1 hour, diluted with CH2Cl2, and washed twice with water. The organic layer was dried with MgSO4 and evaporated. The yield of 4-eq.-chloroadamantylideneadamantane was 300 mg (98%), melting point: 142°-143° C. (literature: 144°-145° C.). 1H NMR (CDCl3): δ 4.15 (br s, 1H); 3.05 (br s 1H); 2.8 (br s, 3H); 2.6-1.15 (br m, 22H) ppm. When 0.1 mmol hydroquinone was added to the solution, exactly the same reaction occurred, and the product could be isolated in virtually the same quantitative yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04705847 |
| Quelldatensatz | uspto-grants-1987_11 |
| ORD ID | ord-32e7d03f339d472298f70a06cd4b7f25 |
| Quellennotiz | uspto-grants-1987_11 |