Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Cresol | HCID 2879 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Chloro-2,4-difluorobenzoic acid | HCID 14876417 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 58042518 | HCID 58042518 | 69.8% |
Reaction Steps
5-Chloro-2,4-difluorobenzoic acid (1.17 g, 6.08 mmol) was dissolved in thionyl chloride (5.0 mL) and heated at 60° C. under a nitrogen atmosphere for 5 hours. The reaction mixture was concentrated in vacuo and azeotroped with DCM (2×10 mL) and toluene (10 mL). Then the crude was dissolved in DCM (15 mL) and cooled to 0° C. 4-Methylphenol (0.665 g, 6.15 mmol) and triethylamine (1.05 mL, 7.53 mmol) in DCM (10 mL) were added dropwise and the reaction mixture was stirred at room temperature under a nitrogen atmosphere for 18 hours. The reaction mixture was concentrated in vacuo and the residue dissolved in EtOAc (10 mL), then washed with saturated aqueous solution of sodium hydrogencarbonate (2×10 mL). The organic layer was dried over sodium sulfate and concentrated in vacuo to yield the crude solid. The solid was triturated in the minimum amount of heptanes to afford the title compound as a white solid (1.20 g, 69%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08592629B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-5a5fa8deee9843c5bde38aa0ab7e1f14 |
|---|
| Source note | uspto-grants-2013_11 |
|---|