HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenyl-5-(trifluoromethyl)thiophene-2-carboxylic acid → 1-[4-phenyl-5-(trifluoromethyl)-2-thienyl]ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenyl-5-(trifluoromethyl)thiophene-2-carboxylic acid | HCID 2783372 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[4-phenyl-5-(trifluoromethyl)-2-thienyl]ethan-1-one | HCID 2740139 | — |
Reaction Steps
To a solution of 4-phenyl-5-trifluoromethyl-thiophene-2-carboxylic acid (272 mg, 1.0 mmol) in THF (10 mL), a solution of MeLi (1.30 mL, 1.6 M solution in diethyl ether) is added. The dark red reaction mixture is stirred at it for 10 min. The reaction is quenched by adding sat. aq. NH4Cl (10 mL). The organic phase is separated, dried over Na2SO4 and evaporated. The crude product is purified by prep. HPLC (Waters Xterra MS18, 75×30 mm, 10 μm, 10 to 95% acetonitrile in water containing 0.5% formic acid) to give 1-(4-phenyl-5-trifluoromethyl-thiophen-2-yl)-ethanone (31 mg) as pale yellow oil, LC-MS: tR=1.06 min, 1H NMR (CDCl3): δ 7.62-7.60 (m, 1H), 7.45-7.40 (m, 5H), 2.60 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951794B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-41fde636b53a4103a83c45270e2c376c |
| Source note | uspto-grants-2011_05 |