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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369492Generated: November 1, 2026

Benzyl Alcohol → 3-(Benzyloxy)-6-chloropyridazine

https://huagongshe.com/reaction/1369492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant3,6-DichloropyridazineHCID 67331—
ReactantSodiumHCID 5360545—
Product3-(Benzyloxy)-6-chloropyridazineHCID 2250695790%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579879B2
Source datasetuspto-grants-2003_06
ORD IDord-61a7a44fce72413c8fb5e3acc571e361
Source noteuspto-grants-2003_06