HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → N-(2-pyridyl)-4-chlorophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | HCID 54187688 | HCID 54187688 | — |
| Solvent | 1,2,3-Trichlorobenzene | HCID 6895 | — |
| Product | N-(2-pyridyl)-4-chlorophthalimide | HCID 4329505 | 84% |
Reaction Steps
5.2 grams of 4-chlorotetrahydrophthalic anhydride, 2.6 grams of 2-aminopyridine, 50 milliliters of trichlorobenzene and 6.0 grams of Calgon Carbon S-Sorb was combined in a 3 neck flask. The flask was fitted with a reflux condenser and an inlet tube adjusted to deliver air as bubbles below the surface. The third neck was fitted with a drying tube to remove water. After about 9 hours, N-(2-pyridyl)-4-chlorophthalimide was formed in about 84% yield as determined by GC-MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06881815B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-94035aa56f0d423395ae981a716e2d53 |
| Source note | uspto-grants-2005_04 |