HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-nitrobenzoic acid → 5-Chloro-2-nitrobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-nitrobenzoic acid | HCID 17286 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Chloro-2-nitrobenzoyl chloride | HCID 2723685 | 104.5% |
Reaction Steps
To a suspension of 5-chloro-2-nitrobenzoic acid (21 g, 100 mmol) in dry methylene chloride (200 mL) at 0° C. were added several drops of DMF, followed by oxalyl chloride (13 mL, 150 mmol). The reaction was warmed to ambient temperature. After 16 hours the solvents were removed and the viscous oil dried in vacuo to afford 23 g (quantitative yield) of 5-chloro-2-nitrobenzoyl chloride; NMR (CDCl3) 8.1 (d, 1), 7.7 (m, 2) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140351 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-334ab236062a4121888a04ebcb61115d |
| Source note | uspto-grants-2000_10 |