HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 2-[(6-Chloropyridazin-3-yl)oxy]ethan-1-amine--hydrogen chloride (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[(6-Chloropyridazin-3-yl)oxy]ethan-1-amine--hydrogen chloride (1/1) | HCID 23313566 | 54.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04599333 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-5c6ef1edb3be4f9d8326bfb04e2e20ab |
| Source note | uspto-grants-1986_07 |