HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 4-Bromo-2-(4-(bromomethyl)benzyl)-1-chlorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | HCID 59557730 | HCID 59557730 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-Bromo-2-(4-(bromomethyl)benzyl)-1-chlorobenzene | HCID 59557743 | — |
Reaction Steps
To a stirred solution of Et3SiH (17 mL) and (5-bromo-2-chlorophenyl)(4-(bromomethyl)phenyl)methanone (intermediate AH) (20.75 g, 54 mmol) in TFA (100 mL) at 30° C. was added CF3SO3H (0.05 mL). Within a few minutes the temperature of the solution increased causing it to reflux violently. After 3 h, the volatiles were removed under reduced pressure. The residue was poured into brine and extracted 3× with ethyl acetate. The combined organic layers were washed 3× with H2O, 2× with aqueous Na2SO4 and 2× with brine, and dried over Na2SO4. The solvent was evaporated under reduced pressure, and the product was purified by column chromatography to obtain pure intermediate AI (15.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575321B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-e78a4695e8e84c4ebc61683d10154646 |
| Source note | uspto-grants-2013_11 |