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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062665Generated: November 2, 2026

Benzene → HCID 22282493, compound

https://huagongshe.com/reaction/1062665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2-fluoroanilineHCID 123050—
Reactant2-(Methylthio)benzeneboronic acidHCID 2773543—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 22282493HCID 2228249381%

Reaction Steps

A benzene solution (100 mL) of 2-methylthiophenylboronic acid (2.07 g, 12.3 mmol); 4-bromo-2-fluoro aniline (1.06 g, 5.6 mmol); aq. Na2CO3 (12.5 mL, 2 M, 25 mmol); and tetra n-butyl ammonium bromide (90 mg, 0.3 mmol) was purged with vacuum and Ar. Bis(triphenylphosphine)palladium (II) chloride (195 mg, 0.3 mmol) was added, and the reaction was refluxed 10 h. After cooling, the reaction was diluted with EtOAc and H2O, the layers were separated, the organic was dried over Na2SO4, filtered, and evaporated. The crude product was chromatographed on silica gel (10% EtOAc/hexanes) to yield the desired product (1.05 g, 81%). 1H NMR (CDCl3) δ: 7.29 (m, 2H); 7.18 (m, 2H); 7.09 (dd, 1H, J=11.7, J′=1.8); 7.01 (dd, 1H, J=8.0, J′=1.4); 6.82 (t, 1H, J=9.2); 3.79 (bs, 2H); 2.38 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962935B2
Source datasetuspto-grants-2005_11
ORD IDord-087932b965d4429985f12785a0a96b8e
Source noteuspto-grants-2005_11