HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-5-nitrobenzoic acid → Benzoyl chloride, 2-chloro-5-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-5-nitrobenzoic acid | HCID 17287 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Product | Benzoyl chloride, 2-chloro-5-nitro- | HCID 117637 | — |
Reaction Steps
To a suspension of 2-chloro-5-nitro-benzoic acid (10 g, 49.6 mmol), oxalyl chloride was added dropwise (12.6 g, 2.0 equiv.). The resulting yellow solution was stirred at room temperature under argon overnight. The solvent was removed under vacuum to give a yellowish solid (10.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919328B1 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-29fbe62ed3984e87a02b69801808aea5 |
| Source note | uspto-grants-2005_07 |