HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 2,6-Dichlorpyridine-3-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2,6-Dichloronicotinic acid | HCID 854047 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-Dichlorpyridine-3-carbonyl chloride | HCID 12263984 | — |
Reaction Steps
To 2,6-dichloropyridine-3-carboxylic acid (75, 1.00 g, 0.00521 mol) in dichloromethane (75 mL) was added 2 M Oxalyl chloride (2.61 mL, 0.727 g, 0.00573 mol). The solution began to show vigorous gas evolution, which slowed but continued for about 2 hours. The reaction was allowed to continue at room temperature for an additional 3 hours. The reaction was concentrated to give the compound as a brown oil that crystallized on standing (76, 1.09 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169250B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-762ede82c929419fbead722cb8681676 |
| Source note | uspto-grants-2015_10 |