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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054725Generated: October 30, 2026

Benzene → Biphenyl

https://huagongshe.com/reaction/2054725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantDodecaneHCID 8182—
ReactantIodobenzeneHCID 11575—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTesmilifene HydrochlorideHCID 175534—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductBiphenylHCID 709585.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

Closed system: To a J. Young NMR tube, in a glove box, was added benzene (437 mg, 5.60 mmol), Ir(COD)(indenyl) (3.0 mg, 0.0070 mmol), dppe (2.8 mg, 0.0070 mmol), dodecane (internal standard, 11.5 mg, 0.0675 mmol), and HBPin (45 mg, 0.352 mmol). The tube was sealed, removed from the box, and stirred at 100° C. for 18 h. The tube was allowed to cool to room temperature and Pd(PPh3)4 (8.1 mg, 0.007 mmol), K3PO4 (112 mg, 0.528 mmol), PhI (72.7 mg, 0.356 mmol), and DME (2 mL) were added. A GC-trace of the reaction mixture revealed PhBPin in 85.7% yield. Three freeze-pump-thaw cycles were performed to remove residual O2 and the reaction mixture was heated at 80° C. for 2 days. GC analysis showed biphenyl (81.8% GC-yield), iodobenzene (7.9.7% GC-conversion), and PhBPin (79.1% GC-conversion).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329769B2
Source datasetuspto-grants-2008_02
ORD IDord-ba935d64a9b94481b738fa748f67859d
Source noteuspto-grants-2008_02