HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 4-Chloropyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 4-chloropyridine-2-carbonyl Chloride | HCID 11095146 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Chloropyridine-2-carboxamide | HCID 303543 | — |
Reaction Steps
Aqueous NH4OH (40%, 250 mL) was added dropwise at 0° C. to a suspension of 4-chloro-pyridine-2-carbonyl chloride (75 g, 533 mmol) in EtOAc. Upon addition, the temperature rose to 30° C. The mixture was stirred for 2 h at RT then kept at RT for 12 h without stirring. MTBE (250 mL) was added to the mixture and the resulting emulsion was filtered. The solid was washed with EtOAc. The MTBE/EtOAc layer was washed twice with water and once with 5% Na2CO3, then dried over MgSO4 and concentrated under vacuum. The resulting solid was suspended in EtOAc several times and filtered out to give the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531553B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-f7398dab32414e60812d91361729e218 |
| Source note | uspto-grants-2009_05 |