HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510819Generated: November 1, 2026
Nitrogen → 6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-carbonitrile
https://huagongshe.com/reaction/510819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | 3-Fluorophenylboronic acid | HCID 2733986 | — |
| Reactant | 6-Acetyl-4-chloro-2-cyano-3-methylphenyl trifluoromethanesulfonate | HCID 58368644 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-carbonitrile | HCID 58368469 | 99% |
Reaction Steps
A biphasic solution of 6-acetyl-4-chloro-2-cyano-3-methylphenyl trifluoromethanesulfonate (2.54 g, 7.4 mmol) and (3-fluorophenyl)boronic acid (1.6 g, 11 mmol) in toluene (70 mL) and saturated sodium bicarbonate (70 mL) was bubbled with N2 to degas. After tetrakis(triphenylphosphine)palladium(0) (0.43 g, 0.37 mmol) was added, the mixture was bubbled with N2 for 5 min more and then heated at 80° C. for 2 hours. After cool to room temperature, 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 to 40% ethyl acetate in hexane, to give the desired product (2.1 g, 99%). LCMS calculated for C16H12ClFNO (M+H)+: m/z=288.1. found: 288.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096600B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-900856663b4b420ca7875ac472ae52b9 |
|---|
| Source note | uspto-grants-2015_08 |
|---|