HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510855Generated: October 31, 2026
Nitrogen → 1-(6-Bromo-4-chloro-5-methylbiphenyl-2-yl)ethanone
https://huagongshe.com/reaction/510855
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 6-Acetyl-2-bromo-4-chloro-3-methylphenyl trifluoromethanesulfonate | HCID 86666786 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 1-(6-Bromo-4-chloro-5-methylbiphenyl-2-yl)ethanone | HCID 86666787 | 93.1% |
Reaction Steps
A biphasic solution of 6-acetyl-2-bromo-4-chloro-3-methylphenyl trifluoromethanesulfonate (3.3 g, 8.3 mmol) and phenylboronic acid (1.2 g, 10 mmol) in toluene (30 mL) and saturated sodium bicarbonate in water (30 mL) was bubbled with N2 to degas. After tetrakis(triphenylphosphine)palladium(0) (0.385 g, 0.333 mmol) was added, the mixture was bubbled with N2 for 5 min. more and heated at 80° C. for 2 hours. After cooling to r.t., the mixture was diluted with ethyl acetate. The layers were separated and the aq. layer was extracted with more ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified on silica gel column, eluting with 0-20% of ethyl acetate in hexane, to give the desired product (2.5 g, 93%). LCMS calculated for C15H13BrClO (M+H)+: m/z=323.0. found: 323.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096600B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-7a08fc72b71d4260ab77c88d1f5e3a76 |
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| Source note | uspto-grants-2015_08 |
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