HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181014Generated: October 31, 2026
Phenylboronic Acid → 3-Chloro-4-methyl-1,1'-biphenyl
https://huagongshe.com/reaction/2181014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-Chloro-4-iodotoluene | HCID 2801329 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 3-Chloro-4-methyl-1,1'-biphenyl | HCID 21651025 | 99.4% |
Reaction Steps
To a suspension of tetrakis(triphenylphosphine)palladium (213 mg) in toluene (7 ml) was added 2-chloro-4-iodotoluene (2.33 g) at room temperature. The mixture was stirred at room temperature for 30 min, and a solution of phenylboronic acid (1.35 g) in ethanol (2 ml) and 2 M aqueous sodium carbonate solution (9.25 ml) were added to this mixture, which was followed by reflux under heating. After 3 hr, the reaction mixture was cooled and the organic layer was separated. The aqueous layer was extracted with hexane (4 ml). The organic layers were combined, washed with saturated aqueous sodium hydrogen carbonate solution (4 ml) and saturated brine (4 ml), and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated. To the residue (2.11 g) were added hexane (10 ml) and silica gel (4 g) and the mixture was stirred at room temperature for 1 hr. Silica gel was filtered off and the filtrate was concentrated to give 2-chloro-4-phenyltoluene as a pale-brown oil (1.86 g, 99.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06890934B2 |
|---|
| Source dataset | uspto-grants-2005_05 |
|---|
| ORD ID | ord-2f83db0feb4644d79665dfbc2c8d6702 |
|---|
| Source note | uspto-grants-2005_05 |
|---|