HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574184Generated: October 30, 2026
3-Chloro-6-methoxypyridazine → 6,6′-Dimethoxy-3,3′-bipyridazine
https://huagongshe.com/reaction/574184
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-6-methoxypyridazine | HCID 74403 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | HCID 178418751 | HCID 178418751 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6,6′-Dimethoxy-3,3′-bipyridazine | HCID 15445190 | 96% |
Reaction Steps
In a 100 ml two-necked flask, 1.55 g (2.1 mmol) of dichlorobis(triphenylphosphine)nickel(II), 452 mg (6.95 mmol) of zinc and 2.23 g (6.95 mmol) of tetrabutylammonium bromide are solubilized in 40 ml of freshly distilled DMF. After degassing, the solution is stirred at ambient temperature for 30 min (the green starting solution turns brown). 1 g (6.95 mmol) of 3-chloro-6-methoxypyridazine 14 is added to this solution, and the reaction mixture is heated at 55° C. for 8 hours. After the solvent has been evaporated off under reduced pressure, the residue is taken up in a saturated solution of ammonium chloride, the suspension is extracted with 4×40 ml of dichloromethane and the organic phase is dried over MgSO4 and then concentrated under reduced pressure. The reaction crude is chromatographed on silica gel (eluent:ethyl acetate/petroleum ether=4/6), to give the bipyridazine 15 with a yield of 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034873B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-c2721166196c4712b317d8935c309cfb |
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| Source note | uspto-grants-2015_05 |
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