HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glyoxal → 6'-Chloro-[2,3']bipyridinyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glyoxal | HCID 7860 | — |
| Reactant | 1,4-Dioxane-2,3-diol | HCID 96170 | — |
| Reactant | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| Product | 6'-Chloro-[2,3']bipyridinyl | HCID 10954361 | 82.5% |
Reaction Steps
The same synthesis procedures as in Example 1 were conducted except for using 2-chloro-5-cyanopyridine and 1,4-dioxane-2,3-diol in place of 4-cyanopyridine and a 40% glyoxal aqueous solution, respectively, and, after completion of the reaction, the organic layer was distilled under reduced pressure of 3.0 to 3.1 Torr to obtain a 150 to 152° C. fraction. Thus, there was obtained 151.0 g (yield: 82.5%) of the end product as pale yellow crystals. HPLC analysis revealed that purity of the product was 99.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06504032B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-79bc5c527b104729a34ea806cfc73a4f |
| Source note | uspto-grants-2003_01 |