HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium hydride → 3-Chloro-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | 2-[(3,6-Dichloro-4-pyridazinyl)oxy]ethanol | HCID 81763547 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Chloro-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazine | HCID 55267440 | — |
Reaction Steps
A solution of 2-[(3,6-dichloro-4-pyridazinyl)oxy]ethanol containing some bromo-derivative (15.46 g; 0.0703 mol) in dry 1,4-dioxane (1.2 L) was treated with lithium hydride (2.3 g; 0.28 mol) in portions and stirred at room temperature for 1 hour under argon, then heated at 110° C. overnight. The reaction mixture was quenched with wet 1,4-dioxane, then iced-water. The solution was evaporated to half volume, taken to pH 8 with 5M hydrochloric acid and evaporated to dryness. Water was added and the residue was extracted 5× with chloroform, dried (sodium sulphate) and evaporated to afford a white solid (12.4 g, ca. 77%) (containing ca. 15% of a bromo species).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071592B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-ca4d08967f634c2f8a23a11454ab98a4 |
| Source note | uspto-grants-2011_12 |