HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 3-(Benzyloxy)-6-chloropyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | 3-(Benzyloxy)-6-chloropyridazine | HCID 22506957 | 90% |
Reaction Steps
Sodium metal (3.1 g) was added to benzyl alcohol (75 mL) and gently warmed to 50° C. for 30 minutes until all the sodium metal dissolved. A solution of 3,6-dichloropyridazine (135 mmol) in benzyl alcohol (75 mL) was added. The reaction mixture was kept at 100° C. for 24 hours. Excess benzyl alcohol was evaporated and the residue was extracted with ethyl acetate (3×100 mL) and the ethyl acetate extract was washed with water. The resulting ethyl acetate layer was collected, dried, filtered, and the filtrate was evaporated to afford the title compound (90%, 26.7 g); mp, 77-78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872722B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-04b8b80673ef4b139af510a6d75deec7 |
| Source note | uspto-grants-2005_03 |