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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113137Generated: October 31, 2026

Toluene → n-((1r)-1-Phenylethyl)[3-(4-methoxyphenyl)-4-methylphenyl]carboxamide

https://huagongshe.com/reaction/2113137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
Reactantn-((1r)-1-Phenylethyl)(3-bromo-4-methylphenyl)carboxamideHCID 681076—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
Productn-((1r)-1-Phenylethyl)[3-(4-methoxyphenyl)-4-methylphenyl]carboxamideHCID 2080322192%

Reaction Steps

To a mixture of N-((1R)-1-phenylethyl)(3-bromo-4-methylphenyl)carboxamide (1.38 g, 4.32 mmol) and 4-methoxyphenylboronic acid (0.53 g, 4.32 mmol) in 10 mL of 2M Na2CO3 aq. soln and 20 mL of toluene was bubbled through N2 for 5 min. Catalyst Pd(PPh3)4 (0.36 g, 0.314 mmol) was then added and the mixture was heated to 80 C for 19 hours under N2. The reaction mixture was cooled to RT and was diluted with 100 mL of EtOAc and 50 mL of water. The organic layer was separated and washed with 50 mL of brine, and dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (CHCl3 to EtOAc) to provide yellow solid (1.0 g, 2.9 mmol, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524873B2
Source datasetuspto-grants-2009_04
ORD IDord-2298c7ba028748b2b5b96a6f9780b26a
Source noteuspto-grants-2009_04