HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 21406355, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 136409735 | HCID 136409735 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 21406355 | HCID 21406355 | 93% |
Reaction Steps
In 50 ml. of acetone was mixed 5 g. of 6-(3,5-dichloro-4-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone obtained in Example 5 and 3.3 g. of anhydrous potassium carbonate and to the resulting mixture was added dropwise 2.4 g. of allyl bromide at room temperature while stirring. After completion of the addition, the mixture was heated under reflux for 4 hours. After cooling, the reaction mixture was filtered, the filtrate was concentrated under reduced pressure and the residue was recrystallized from ethanol to give 5.3 g. of the desired product of m.p. 137° C. (Yield 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04052395 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-4f0beae55e124702a35f894fd2d25a70 |
| Source note | uspto-grants-1977_10 |