HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → HCID 66914131, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178515289 | HCID 178515289 | — |
| Reactant | HCID 178515327 | HCID 178515327 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66914131 | HCID 66914131 | 59% |
Reaction Steps
3-Phenyl-8-(trifluoromethyl)quinolin-4-ol: A solution of 3-bromo-8-(trifluoromethyl)quinolin-4-ol (3.2 g, 10.95 mmol) and phenyl boronic acid (2.67 g, 21.91 mmol) in 2:1 toluene:methanol (120 mL) and sat aq NaHCO3 (40 mL) is treated with Pd(PPh3)4 (760 mg) and heated at reflux overnight. The reaction is poured into water and extracted with ethyl acetate. The combined extracts are washed with 2N aq NaOH, water, brine, and dried with magnesium sulfate. The extracts are concentrated and the residue is chromatographed with 1:4 ethyl acetate:hexanes to afford the title compound as a yellow solid (6.4 g, 59%). mp 272-275° C.; MS (ESI) m/z 290; MS (ESI) m/z 288; HRMS: calcd for C16H10NF3O+H, 290.07927; found (ESI_FT, [M+H]1+), 290.07816.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576215B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-30ce3a9722704f9ab6f3e0aa966074c7 |
| Source note | uspto-grants-2009_08 |