Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246591Generated: October 30, 2026

4-Bromotoluene → 2-Methoxy-4'-methyl-1,1'-biphenyl

https://huagongshe.com/reaction/1246591

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromotolueneHCID 7805—
ReactantSodium CarbonateHCID 10340—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
ReactantN-butyl-ammonium bromideHCID 21904131—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-Methoxy-4'-methyl-1,1'-biphenylHCID 1031354181%

Reaction Steps

4-bromotoluene, 171 mg (1 mmol), 2-methoxyphenylboronic acid, 152 mg (1 mmol), palladium diacetate, 1 mg (4 μmol), N-butylammonium bromide, 322 mg (1 mmol), and 2 M aqueous Na2CO3, 1.9 mL (3.8 mmol), were placed in a microwaveable pressure vial and heated to 150 C for 5 minutes. After cooling to room temperature, the product was poured into a separatory funnel and 30 mL each of water and diethyl ether were added. After extraction, the layers were separated and the aqueous layer washed with another 30 mL diethyl ether. The ether extracts were combined, dried over MgSO4, and the solvent removed by rotary evaporation under vacuum. 2-methoxy-4′-methylbiphenyl, 160 mg (81% yield) was obtained as a solid product, 95% purity by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129215B2
Source datasetuspto-grants-2006_10
ORD IDord-ce140f9a70ba4c849c37bf04ec60c00c
Source noteuspto-grants-2006_10