HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triisopropyl borate → 2-Methoxy-5-(trifluoromethyl)phenylboronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 2-iodine-4 -(trifluoromethyl) anisole | HCID 18706296 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-5-(trifluoromethyl)phenylboronic acid | HCID 2782676 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
n-Butyl lithium (1.6M in hexanes, 456 μL, 0.729 mmol) was added dropwise to a stirred solution of 2-iodo-1-methoxy-4-(trifluoromethyl)benzene (Step A, 200 mg, 0.662 mmol) in THF (1.5 mL) at −78° C. under an atmosphere of nitrogen. The reaction stirred at −78° C. for 30 min prior to the addition of triisopropyl borate (458 μL, 1.986 mmol). The reaction stirred an additional 2 h at −78° C. and was quenched with sat. NH4Cl. The mixture was extracted with CH2Cl2 and the organic phase was washed with NaHCO3 (15 mL) and brine (15 mL), dried (Na2SO4), filtered, conc. in vacuo to afford [2-methoxy-5-(trifluoromethyl)phenyl] boronic acid which was carried on without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652049B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-0412635863374b26869bb505e5c3d4c0 |
| Source note | uspto-grants-2010_01 |