HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 3-bromo-1-(3,5-dichloropyridin-2-yl)-1H-pyrazole-5-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-bromo-1-(3,5-dichloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid | HCID 58158930 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromo-1-(3,5-dichloropyridin-2-yl)-1H-pyrazole-5-carbonyl chloride | HCID 58158929 | 100% |
Reaction Steps
To a 100 mL flask, 3-bromo-1-(3,5-dichloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid (0.4 g, 1.2 mmol), dichloromethane (10 mL) and oxalyl dichloride (0.31 g, 2.4 mmol) were added. After five drops of N,N-dimethyl formamide was added, a large number of gas was released. After being stirred for 8 hours at room temperature, the reaction mixture was evaporated to dryness at reduced pressure. Then toluene (100 mL) was added, and the reaction mixture was concentrated again under vacuum to give the product (0.42 g) as green solid in 100% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492409B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-14505f5a164b4ab4bc8ed155a593d42e |
| Source note | uspto-grants-2013_07 |