HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium iodide → 2,6-Dichloro-4-(methylcarbamoyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | Methyl 2,6-dichloro-4-(methylcarbamoyl)benzoate | HCID 71061695 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2,6-Dichloro-4-(methylcarbamoyl)benzoic acid | HCID 71061633 | — |
Reaction Steps
A well stirred mixture of methyl 2,6-dichloro-4-(methylcarbamoyl)benzoate (280 mg, 1 mmol, Step a) and anhydrous lithium iodide (429 mg, 3.2 mmol) in pyridine (3 mL) was heated under reflux for 3 hours. The reaction mixture was concentrated under vacuum to remove pyridine. The residue was acidified using ice-cooled dilute hydrochloric acid solution and partitioned with ethyl acetate. The combined organic layer was washed with brine, dried over sodium sulfate, and concentrated under vacuum to obtain a solid that upon triturating with cold diethyl ether yielded pure 2,6-dichloro-4-(methylcarbamoyl)benzoic acid (200 mg, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09364466B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-84d647545a7b4a7caee40f9bac04290b |
| Source note | uspto-grants-2016_06 |