HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 3-Fluoro-4-phenoxybenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 3,4-Difluorobenzaldehyde | HCID 588088 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Product | 3-Fluoro-4-phenoxybenzoic acid | HCID 28605115 | 94.7% |
Reaction Steps
The title compound (1.1 g) was synthesized in a yield of 93% as a white crystalline solid by conducting a reaction similar to that mentioned in Example 10 (10e) using 3,4-difluorobenzaldehyde (0.71 g, 5.0 mmol), phenol (0.56 g, 6.0 mmol), potassium carbonate (1.4 g, 10 mmol), 2-methyl-2-butene (2.5 mL, 23 mmol), potassium dihydrogenphosphate (1.6 g, 12 mmol), and sodium hypochlorite (1.3 g, 14 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687491B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-c3eb2dfcbb2b4ef6b2dbb3387365b606 |
| Source note | uspto-grants-2010_03 |