HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → HCID 14798950, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Benzoylacetonitrile | HCID 64799 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14798950 | HCID 14798950 | 20.9% |
Reaction Steps
1 g (7 mmol) of α-cyanoacetophenone, 8 g (43 mmol) of 1,2-dibromoethane, 0.1 g (0.4 mmol) of 18-crown-6 and 4 g (69 mmol) of potassium fluoride are heated under reflux for 18 h as a heterogeneous system in 10 ml of dichloromethane. After cooling, the mixture is filtered, the organic phase is washed with H2O and the solvent is evaporated in vacuo after drying over Na2SO4. The residue is chromatographed on a silica gel using CH2Cl2. 0.25 g (20% of theory) of 1-benzoyl-1-cyanocyclopropane are obtained in this manner as a colorless oil,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05059615 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-d1f5cbc4f007424b8ec05e31f4af6a49 |
| Source note | uspto-grants-1991_10 |