HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → Quinoline-3-carbonyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Quinoline-3-carboxylic acid | HCID 80971 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Quinoline-3-carbonyl Chloride | HCID 11030631 | — |
Reaction Steps
To a suspension of 3-quinolinecarboxylic acid (580 mg, 3.35 mmol) in dichloromethane (25 mL) was added oxalyl chloride (2M in CH2Cl2, 3.4 mL, 6.7 mmol) dropwise at room temperature. DMF (1 drop) was added, resulting in immediate gas formation. The reaction mixture was stirred at room temperature for 2 h. Dichloromethane was evaporated. Additional dichloromethane (20 mL) was added to the residue. Concentration of the organic solvent gave the crude product. (640 mg, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06613747B2 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-cf4121c1fd5540f6baa7d4341bdba3b1 |
| Source note | uspto-grants-2003_09 |