HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium iodide → 2,6-Dichloro-4-cyanobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | Methyl 2,6-dichloro-4-cyanobenzoate | HCID 53401291 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2,6-Dichloro-4-cyanobenzoic acid | HCID 17855060 | 86% |
Reaction Steps
A suspension of methyl 2,6-dichloro-4-cyanobenzoate (620 mg, 2.6 mmol) in pyridine (5 mL) was treated with anhydrous lithium iodide (1000 mg, 8 mmol). The resulting reaction mixture was stirred at reflux for 1 hour and concentrated under vacuum to remove pyridine. The residue was acidified with hydrochloric acid (2N) under ice-cold condition to adjust the pH between 2 to 3. The precipitated solid was filtered, washed with water and dried to yield 2,6-dichloro-4-cyanobenzoic acid (380 mg, 86%) as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09364466B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-babceb7a2ed049cdb78f2ede04bc99de |
| Source note | uspto-grants-2016_06 |