HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → (3-Benzyloxy-5-trifluoromethyl-phenyl)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Fluoro-5-(trifluoromethyl)phenylacetic acid | HCID 2759172 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | (3-Benzyloxy-5-trifluoromethyl-phenyl)-acetic acid | HCID 59644613 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To 3-fluoro-5-(trifluoromethyl)phenylacetic acid (2.0 g, 9.0 mmol) and benzyl alcohol (1.9 mL, 18.0 mmol) in NMP (10 mL) was added sodium hydride (60% in mineral oil; 0.8 g, 19.8 mmol), and the reaction was stirred at 120° C. for 3 hours. The mixture was acidified and extracted with EtOAc, and the crude material was purified by silica gel chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362044B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-2f953c3c988b41f88870239a3573e9fa |
| Source note | uspto-grants-2013_01 |