HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927121Generated: October 31, 2026
Cesium carbonate → HCID 86677036, compound
https://huagongshe.com/reaction/927121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Chloro-1,2-bis(trifluoromethyl)benzene | HCID 45790480 | — |
| Reactant | HCID 86677037 | HCID 86677037 | — |
| Product | HCID 86677036 | HCID 86677036 | — |
Reaction Steps
3,4-bis(Benzyloxy)-6-ethenylpyridazine (Intermediate 78: 0.578 g, 1.816 mmol), cesium carbonate (0.887 g, 2.72 mmol), dichloropalladiumtricyclohexylphosphane (1:2) (0.067 g, 0.091 mmol) and 4-chloro-1,2-bis(trifluoromethyl)benzene (0.542 g, 2.179 mmol) were combined. The reaction vessel was evacuated and purged with nitrogen before toluene (6.05 ml) was added under vacuum and the whole was stirred under nitrogen and heated to 140° C. for 11 hours. Upon quenching with saturated aqueous ammonium chloride, the resulting mixture was diluted with dichloromethane, passed through a phase separator and concentrated in vacuo. The residue was purified by column chromatography eluting (silica, 0-50% ethyl acetate in petrol) to yield crude 3,4-bis(benzyloxy)-6-[(E)-2-[3,4-bis(trifluoromethyl)phenyl]-ethenyl]-pyridazine which was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290456B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-79310324b0e6458496d474097288e065 |
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| Source note | uspto-grants-2016_03 |
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