HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 21450232, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19884680 | HCID 19884680 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 21450232 | HCID 21450232 | — |
Reaction Steps
i. A stirred mixture of finely powdered 6-(3-hydroxyphenyl)-4,5-dihydro-3(2H)-pyridazinone (13.1g, 0.07 mole), potassium carbonate (9.5g, 0.07 mole), allyl bromide (11.75 ml, 0.14 mole), and dry acetone (250 ml) was heated under reflux for 18 hours. Evaporation of the filtered solution under reduced pressure gave 6-(3-allyloxyphenyl)-4,5-dihydro-3(2H)-pyridazinone which was washed with ether (13.66g, 86%, m.p. 111°-113° C). Crystallisation from a small volume of ethanol gave the pure pyridazinone m.p. 112°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04011321 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-5727f5626a58456fa1420ebabdb7bbac |
| Source note | uspto-grants-1977_03 |