HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl borate → [2,6-Dimethoxy-4-(1-methoxyethyl)phenyl]boronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromo-1,3-dimethoxy-5-(1-methoxyethyl)benzene | HCID 58223419 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2,6-Dimethoxy-4-(1-methoxyethyl)phenyl]boronic acid | HCID 58223453 | 77% |
Reaction Steps
To a tetrahydrofuran (200 ml) solution of 2-bromo-1,3-dimethoxy-5-(1-methoxyethyl)benzene (7.39 g, 26.9 mmol), was added dropwise 1.57M n-butyl lithium (18.8 ml, 29.6 mmol) at −78° C., and the mixture was stirred for 30 minutes. To the mixture, was added dropwise trimethyl borate (6.00 ml, 53.8 mmol), and warmed to room temperature. After the reaction was completed, a saturated aqueous solution of ammonium chloride was added while cooling on ice, which was extracted with ethyl acetate and dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-heptane/ethyl acetate=1/1) to obtain the title compound (4.97 g, 20.7 mmol)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530504B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-63ab5f25dd144985a5ddcef1d408e7c9 |
| Source note | uspto-grants-2013_09 |