HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → 7-Bromo-4-chloro-5-(4-ethoxybenzyl)-2-methyl-2,3-dihydrobenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | (7-Bromo-4-chloro-2-methyl-2,3-dihydrobenzofuran-5-yl)(4-ethoxyphenyl)methanone | HCID 71078368 | — |
| Solvent | Acetonitrile methylene chloride | HCID 21877088 | — |
| Product | 7-Bromo-4-chloro-5-(4-ethoxybenzyl)-2-methyl-2,3-dihydrobenzofuran | HCID 71076922 | 88.2% |
Reaction Steps
To a solution of crude methanone 89 (3.15 g, 7.96 mmol) in CH2Cl2/CH3CN (25 mL/25 mL) were added triethylsilane (3.8 mL, 23.9 mmol) and boron trifluoride diethyl etherate (3.0 mL, 23.9 mmol) at 0° C. The mixture was warmed up to room temperature slowly and stirred at room temperature for 15 hours. To the mixture was added aq. saturated K2CO3 solution (70 mL) slowly and extracted with EtOAc (50 mL×2). The combined organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by normal phase column chromatography to provide the desired product 90 (2.68 g, 85% (2-steps)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034921B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-855b92a10528405eae09f28404f6a669 |
| Source note | uspto-grants-2015_05 |