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 (x3). 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 | US09062048B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-c2a5e4b325de4dbda9c8a0b76d1dfe8a |
| Source note | uspto-grants-2015_06 |