HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375058Generated: October 27, 2026
Potassium Carbonate → HCID 18994137, compound
https://huagongshe.com/reaction/375058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-5-methoxypyridazine | HCID 10975612 | — |
| Reactant | HCID 178516524 | HCID 178516524 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 18994137 | HCID 18994137 | 45% |
Reaction Steps
2-Difluoromethoxy-4-hydroxypyridine (123 g, 0.764 mol), 3-chloro-5-methoxypyridazine (110.47 g, 0.764 mol), potassium carbonate (211.18 g, 1.53 mol), CuBr (54.80 g, 0.382 mol) and 18-crown-6 (1 g) were mechanically stirred under nitrogen in diglyme (1.28 L) at 100° C. for 30 h. The mixture was cooled to RT and partitioned between ethyl acetate and 2 L of 3% HCl. The layers were separated. The aqueous layer was then adjusted to pH--1 with conc. HCl and extracted twice with additional ethyl acetate. The combined organics were filtered through silica gel and then extracted twice with 1.5 N NaOH. Solids were formed which were removed by filtering the organic layer through silica gel and celite. The organic layer was dried (MgSO4), filtered through silica gel and evaporated in-vacuo. The residue was triturated with ethyl acetate and filtered to give pure 3-[[2-(difluoromethoxy)-4-pyridinyl]oxy]-5-methoxypyridazine (92.5 g, 45% yield) as a light brown solid, mp=119° C. -120.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05484761 |
|---|
| Source dataset | uspto-grants-1996_01 |
|---|
| ORD ID | ord-7b486cb0db3a43e0942854b711915592 |
|---|
| Source note | uspto-grants-1996_01 |
|---|