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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745502Generated: October 31, 2026

Ethanolamine → 2-[(6-Chloropyridazin-3-yl)oxy]ethan-1-amine--hydrogen chloride (1/1)

https://huagongshe.com/reaction/745502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantSodium hydrideHCID 24758—
Reactant3,6-DichloropyridazineHCID 67331—
SolventBenzeneHCID 241—
Product2-[(6-Chloropyridazin-3-yl)oxy]ethan-1-amine--hydrogen chloride (1/1)HCID 2331356654.2%

Reaction Steps

To a suspension of 4.2 g of 61% sodium hydride in 100 ml of benzene was added dropwise 6.2 g of 2-aminoethanol at room temperature. Then, 15 g of 3,6-dichloropyridazine was added, and the mixture was refluxed for 1 hour. After cooling, the reaction mixture was washed with water, and dried over magnesium sulfate. After evaporating the solvent, the residue was treated with hydrogen chrolide-ether solution to give 5.73 g of 3-(2-aminoethoxy)-6-chloropyridazine hydrochloride as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04599333
Source datasetuspto-grants-1986_07
ORD IDord-5c6ef1edb3be4f9d8326bfb04e2e20ab
Source noteuspto-grants-1986_07