HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2,4'-Bipyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Acetylpyridine | HCID 14282 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tetramethoxypropane | HCID 66019 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Catalyst | 1-Methyl-3-phenylurea | HCID 13880 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2,4'-Bipyridine | HCID 68488 | 63.2% |
Reaction Steps
12.3 g (79 mmol) of 1,1,3,3-tetramethoxypropane, 0.12 g (0.8 mmol) of 1-methyl-3-phenylurea, 9.6 g (79 mmol) of 4-acetylpyridine, 30 ml (500 mmol) of acetic acid and 39 g (500 mmol) of ammonium acetate were dissolved in 160 ml of 2-propanol, and the reaction solution was allowed to undergo the reaction at 80° C. for 9 hours. After completion of the reaction, this was cooled to room temperature, neutralized with 200 g (1.2 mol) of 25% sodium hydroxide aqueous solution and then extracted three times with 200 ml of toluene. The organic layer was concentrated and then purified by distillation under a reduced pressure to obtain 7.8 g (yield 63.2%) of the title compound (purity 99.2%, melting point 55-57° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723522B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-dcce16a8d3a74ce09ed7aa03c9bb39ec |
| Source note | uspto-grants-2010_05 |