HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 1-Phenoxy-7-(trifluoromethyl)isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Chloro-7-(trifluoromethyl)isoquinoline | HCID 58562677 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Phenoxy-7-(trifluoromethyl)isoquinoline | HCID 58562471 | — |
Reaction Steps
A mixture of 1-chloro-7-(trifluoromethyl)isoquinoline (1.5 g, 6.5 mmol), from above step C, KOH (0.73 g, 13 mmol) and phenol (6.1 g, 65 mmol) were heated at 100° C. for 72 h. The resulting mixture was cooled to room temperature and taken in Et2O and extracted with 4N NaOH (×3). The organic fraction was washed with water, saturated NaCl, dried over Na2SO4 and evaporated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518969B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-6c8ddd4d79be494b831179c52962f754 |
| Source note | uspto-grants-2013_08 |