HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroaniline → HCID 67958530, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroaniline | HCID 7240 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | Ethyl 5-ethoxypicolinate | HCID 67958698 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67958530 | HCID 67958530 | — |
Reaction Steps
To a solution of o-chloroaniline (0.68 g, 5.3 mmol) in 20 mL of PhMe was added 3 mL of AlMe3. The mixture was stirred at ambient temperature for 0.5 h and added into a solution of ethyl 5-ethoxypyridine-2-carboxylate 3 (0.26 g, 1.33 mmol) in 10 mL of PhMe. The mixture was stirred at ambient temperature for 15 h and quenched with 20 mL of 1N HCl. The mixture was extracted with ethyl acetate. The organic layer was separated and concentrated. The residue was purified by column (2:1 of hexane/ethyl acetate) to give N-(2-chlorophenyl)-5-ethoxypyridine-2-carboxamide 4 as a solid. Yield: 310 mg, 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403812B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-9030c4beb75440eea619a6bd91dc7c4c |
| Source note | uspto-grants-2016_08 |