HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875242Generated: October 31, 2026
Cesium carbonate → HCID 86650769, compound
https://huagongshe.com/reaction/875242
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Bromo-6-(bromomethyl)pyridine | HCID 12954796 | — |
| Reactant | HCID 136331258 | HCID 136331258 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86650769 | HCID 86650769 | 90.5% |
Reaction Steps
To a stirred solution of N-hydroxy-1-(4-methyl-4H-1,2,4-triazol-3-yl)-1-phenylmethanimine (0.45 g, 2.22 mmol, 1.0 eq.) in 20 ml of MeCN was added Cs2CO3 (0.795 g, 2.44 mmol, 1.1 eq.) followed by Kl (0.0365 g, 0.22 mmol, 0.1 eq.) in one portion. The resulting suspension was stirred for 5 mins before addition of 2-bromo-6-(bromomethyl)pyridine (0.586 g, 2.33 mmol, 1.05 eq.) in one portion. The reaction was stirred for 4 h at room temperature. The solid was removed by filtration and washed with 250 ml of fresh MeCN. The filtrate was evaporated, and 500 ml of EtOAc were added. The organic layer was washed with H2O and dried over MgSO4 then concentrated. Chromatography of the crude on silica gel gave N-[(6-bromopyridin-2-yl)methoxy]-1-(4-methyl-4H-1,2,4-triazol-3-yl)-1-phenylmethanimine (0.748 g, 90% yield) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08981111B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-0f1e69ad048749cdba47e0f4ccafb964 |
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| Source note | uspto-grants-2015_03 |
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