HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 4-Bromo-1-chloro-2-(4-ethoxy-benzyl)-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | (5-Bromo-2-chlorophenyl)(4-ethoxyphenyl)methanone | HCID 10020105 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-Bromo-1-chloro-2-(4-ethoxy-benzyl)-benzene | HCID 9996449 | 94.4% |
Reaction Steps
To (5-bromo-2-chlorophenyl)(4-ethoxyphenyl)methanone (1440 g, 4.26 mol) and triethylsilane (1.37 L, 8.6 mol) in trifluoroacetic acid (820 mL) was slowly added trifluoromethanesulfonic acid (1.9 mL). After refluxing for 6 hours, additional triethylsilane (400 mL, 2.47 mol) was added. After refluxing for another 8 hours, the mixture was evaporated under reduced pressure. The residue was dissolved in dichloromethane (20 L), washed with water (10 L), aqueous sodium carbonate (10 L), and brine (10 L), and concentrated to give crude product. The crude product was distilled to remove (Et3Si)2O under vacuum. The residue was recrystallized from absolute ethanol (5 L) and dried under vacuum to give compound 3 (1310 g, 94% yield, HPLC purity>99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09061060B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-e231fa2d300b41a2b9f45406e73474d0 |
| Source note | uspto-grants-2015_06 |