HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 23117635, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 58696280 | HCID 58696280 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23117635 | HCID 23117635 | 94.2% |
Reaction Steps
Ethyl(benzylidene-amino)-(3,4-dichlorophenyl)-acetate (1.41 mol) was dissolved in ethyl acetate (2.3 L). Allyl bromide (341 g), potassium carbonate (390 g), and tetrabutylammonium bromide (45 g) were added to the resultant mixture, followed by refluxing for 2.5 hours. The reaction mixture was left to cool to room temperature. The mixture was sequentially washed with water and saturated brine, dried over sodium sulfate anhydrate, and concentrated under reduced pressure, to thereby give the title compound (500 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276511B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-0e63fdad07464e2ba3a1878b7b301eee |
| Source note | uspto-grants-2007_10 |