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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371245Generated: October 30, 2026

Sodium Carbonate → HCID 53443277, compound

https://huagongshe.com/reaction/2371245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-IodoanilineHCID 10893—
ReactantBenzo[b]furan-2-boronic acidHCID 2776266—
SolventDimethoxyethane ethanol waterHCID 86587095—
ProductHCID 53443277HCID 5344327799.6%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 4-iodo-aniline (25.0 g, 114.1 mmol), 2-benzofuran-boronic acid (27.7 g, 171.2 mmol), PdCl2(O-tolylphosphine) (11.66 g, 14.8 mmol), and Na2CO3 (60.49 g, 570.7 mmol) in DME/EtOH/H2O (4:2:1) (700 mL) was heated at 125° C. for 2 h. The reaction mixture was cooled to room temperature, filtered and washed. The solvent was removed under reduced pressure. The residue was partitioned (ethyl acetate/water) and the organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The resulting crude was purified by column chromatography on silica gel, eluting with dichloromethane to afford 4-benzofuran-2-yl-phenylamine (11) as a pale yellow solid (23.78 g, 99.5%): 1H NMR (300 MHz, CDCl3): δ 7.66 (d, J=9.0 Hz, 2H), 7.51-7.55 (m, 2H), 7.20-7.23 (m, 2H), 6.81 (s, 1H), 6.73 (d, J=9.0 Hz, 2H), 3.83 (bs, 2H) TLC conditions: Uniplate silica gel, 250 microns; mobile phase=ethyl acetate/hexanes (2:1); Rf=0.45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710236B2
Source datasetuspto-grants-2014_04
ORD IDord-58f20b48887d442eb3530a8dacb06e98
Source noteuspto-grants-2014_04