HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510913Generated: October 25, 2026
(3,5-Difluorophenyl)boronic acid → 1-(6-Bromo-4-chloro-3',5'-difluorobiphenyl-2-yl)ethanone
https://huagongshe.com/reaction/510913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3,5-Difluorophenyl)boronic acid | HCID 2734338 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Acetyl-6-bromo-4-chlorophenyl trifluoromethanesulfonate | HCID 86666832 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(6-Bromo-4-chloro-3',5'-difluorobiphenyl-2-yl)ethanone | HCID 67969272 | 89.2% |
Reaction Steps
A solution of sodium hydrogenecarbonate (2.0 g, 23 mmol) in water (50 mL) was treated with a solution of 2-acetyl-6-bromo-4-chlorophenyl trifluoromethanesulfonate (4.5 g, 12 mmol) in toluene (50 mL) followed by (3,5-difluorophenyl)boronic acid (2.0 g, 13 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.67 g, 0.58 mmol). The reaction mixture was degassed with nitrogen for 5 min and heated at 80° C. overnight. The reaction mixture was diluted with water and extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with sodium bicarbonate, water, and brine, dried with sodium sulfate, filtered, and concentrated to a crude residue. Purification by flash column chromatography using ethyl acetate in hexanes (0%-10%) gave the desired product (3.7 g, 82%). LCMS for C14H9BrClF2O (M+H)+: m/z=344.9, 346.9. Found: 344.9, 346.8.
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-d0747f37c2e0470a905b96db01b1c0a7 |
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| Source note | uspto-grants-2015_08 |
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