HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1-Bromo-1-chloroethane → 1-(3,4-Dichlorophenyl)cyclopropanecarbonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1-Bromo-1-chloroethane | HCID 11654 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | (3,4-Dichlorophenyl)acetonitrile | HCID 76690 | — |
| Katalysator | Benzyl triethylammonium chloride | HCID 66133 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(3,4-Dichlorophenyl)cyclopropanecarbonitrile | HCID 11600939 | 102,4% |
Reaktionsschritte
To a stirred mixture of 3,4-Dichloro-phenylacetonitrile (4.65 g. 25 mmol) triethylbenzylammonium chloride (0.2 g) and 1-bromochoroethane (4.2 ml, 50 mmol), 50% sodium hydroxide (16 ml, 200 mmol) was added dropwise at 50° then the reaction was stirred at 50° for 10 hrs. After cooling to rt, the reaction mixture was diluted with water and extracted with EtOAc (×3). The layers were separated, washed with water (×3) and brine, then dried over MgSO4. Evaporation of the solvent under reduced pressure afforded the title compound (5.43 g) which was then recrystallized from Et2O/hexanes as a pale pink solid (4.49 g, 85%). Lc/MS(ES) m/e 212 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07427623B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-fd1e2f70ca8f4ed298ab9deca05721ae |
| Quellennotiz | uspto-grants-2008_09 |