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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216030Generated: October 31, 2026

Ethanol → 6-Methyl-biphenyl-3-ylamine

https://huagongshe.com/reaction/2216030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantBenzenamine, 3-bromo-4-methyl-HCID 82187—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product6-Methyl-biphenyl-3-ylamineHCID 1224780047.1%

Reaction Steps

To a dried flask was added 3-bromo-4-methyl-phenylamine (1 g, 5.37 mmol), phenyl boronic acid (2.62 g, 21.5 mmol), aqueous Na2CO3 (2M, 21.5 mL, 43 mmol), ethanol (21.5 mL), and toluene (43 mL). The flask was sparged with Ar, and Pd(PPh3)4 (1.55 g, 1.34 mmol) was added. The reaction mixture was stirred and heated at 80° for 18 hrs, then cooled to room temperature. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate. The organic layer was washed with water and brine, then dried over MgSO4. The solvent was removed in vacuo and the residue was purified via column chromatography (SiO2, 5% DCM/hexane) to afford a yellow oil (463 mg, 47%). This was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109354B2
Source datasetuspto-grants-2006_09
ORD IDord-fa08c0cb10ba4c6c818c18fb37271f36
Source noteuspto-grants-2006_09