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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376939Generated: October 29, 2026

1-Fluoro-2-iodobenzene → HCID 21099473, compound

https://huagongshe.com/reaction/2376939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-iodobenzeneHCID 67673—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantHCID 21099480HCID 21099480—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
SolventAcetonitrile triethylamineHCID 21895542—
ProductHCID 21099473HCID 2109947357.4%

Reaction Conditions

Temperature170 °C

Reaction Steps

2-Vinyl-5-[(2-fluorophenyl)sulfonyl]pyridine (Step 1, 50 mg, 0.19 mmol), 2-fluoroiodobenzene (46 mg, 0.207 mmol), palladium(II) acetate (2 mg, 0.01 mmol) and tri-o-tolylphosphine (12 mg, 0.039 mmol) were taken up in acetonitrile/triethylamine (0.5 mL/0.5 mL) and the reaction heated to 170° C. for 20 minutes in a Smith synthesiser microwave reactor. The reaction was diluted with ethyl acetate and washed with saturated aqueous ammonium chloride solution. The organic layers were dried over MgSO4 and concentrated in vacuo. The residue was purified by mass-triggered preparative HPLC (Nebula) to give the title compound as a beige solid (39 mg, 57%). δH (500 MHz, d6 DMSO): 9.03 (1H, d, J=2.2 Hz), 8.28 (1H, dd, J=1.6, 8.3 Hz), 8.05 (1H, td, J=7.6, 1.6 Hz), 7.92 (1H, d, I=16.1 Hz), 7.84 (1H, td, J=8.0, 1.4 Hz), 7.80-7.74 (2H, m), 7.47 (1H, d, J=16.1 Hz), 7.47 (1H, d, =0.7 Hz), 7.42-7.36 (2H, m), 7.27-7.21 (2H, m); m/z (ES+) 358 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468393B2
Source datasetuspto-grants-2008_12
ORD IDord-341ec42a8d344d80bd704c9b741c928a
Source noteuspto-grants-2008_12