HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-[2-Hydroxy-4-(trifluoromethyl)phenyl]ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Hydroxy-4-(trifluoromethyl)benzoic acid | HCID 164578 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[2-Hydroxy-4-(trifluoromethyl)phenyl]ethan-1-one | HCID 15446449 | — |
Reaction Steps
A solution of 2-hydroxy-4-(trifluoromethyl)benzoic acid (10.0 g, 48.5 mmol) and THF (100 mL) was cooled to <5° C. and methyllithium (95 mL, 1.6M solution in diethyl ether, 152 mmol) was slowly added, keeping the internal temperature <20° C. The resulting solution was warmed to ambient temperature and stirred for 1 hour. The solution was then cooled to 10° C. and treated carefully with EtOAc (100 mL) and 2N HCl (100 mL). The reaction mixture was further diluted with EtOAc (100 mL) then washed with water (100 mL) and brine (20 mL). The organic portion was dried (Na2SO4), filtered, and concentrated to give the title compound (10.3 g). This material was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859584B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-8de4664b1b0e4a0f9b9e167bc9f61ea6 |
| Source note | uspto-grants-2014_10 |