HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101469Generated: October 30, 2026
Benzyl Alcohol → 3-(Benzyloxy)-6-chloropyridazine
https://huagongshe.com/reaction/2101469
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 (130 mmol, 3.1 g) was added to benzyl alcohol (75 mL) and gently warmed to 50° C. for 30 minutes until all the sodium metal had dissolved. To this was added a solution of 3,6-dichloropyridazine (135 mmol) in benzyl alcohol (75 mL). The reaction was heated at 100° C. for 24 h. Excess benzyl alcohol was evaporated and the residue was extracted with EtOAc (3×100 mL). The EtOAc extract was washed with H2O. The EtOAc layer was collected, dried, filtered and the filtrate was evaporated to yield 3-benzyloxy-6-chloro-pyridazine (90%, 26.7 g); mp 77° C.-78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572910B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-9adb7f9eac3b4244ad2e58d9ec8c26f6 |
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| Source note | uspto-grants-2009_08 |
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