HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 66914340, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Phenyl[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanone | HCID 11360909 | — |
| Reactant | Orthoformate | HCID 21585117 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66914340 | HCID 66914340 | 813.4% |
Reaction Steps
phenyl[4-phenyl-8-(trifluoromethyl)quinolin-3-yl]methanone (0.210 g, 0.56 mmol) in MeOH (5 mL) is refluxed with trimethylorthoformate (0.12 mL, 1.12 mmol) and para-toluenesulfonic acid (0.005 g). After 5 h, additional orthoformate (0.20 mL) is added. After 3 h more, more orthoformate (0.20 mL) is added. After refluxing overnight, the reaction is cooled and treated with NaOMe in methanol (0.5 mL). After 10 min of stirring, the reaction is concentrated and the residue chromatographed eluting with 5:95 ethyl acetate:hexanes to afford the title compound as a white solid (0.100 g). MS (ESI) m/z 424; HRMS: calcd for C25H20F3NO2+H, 424.15244; found (ESI, [M+H]+), 424.1519.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576215B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-daf870e75383467292a3eaf1ef4535ac |
| Source note | uspto-grants-2009_08 |