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 | 73.4% |
Reaction Steps
To a solution of methyl 2,6-dichloro-4-cyanobenzoate (160 g, 694 mmol) in pyridine (1.5 L) at room temperature was added LiI (186 g, 1.39 mol). The mixture was heated under reflux for 2 hours, cooled to room temperature and concentrated under reduced pressure. The residue was treated with 2 N HCl (1 L) and the resulting precipitate was collected by filtration. The solid was recrystallized from DMF and water to give 2,6-dichloro-4-cyanobenzoic acid (110 g, yield: 73%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 8.18 (s, 2H). LCMS (ESI) m/z: 216.0 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486950B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-4f2ecd09651e4eaaa37edec68de86fe4 |
| Source note | uspto-grants-2013_07 |