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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701008Generated: October 30, 2026

Sodium Carbonate → 2-Methyl-4-nitro-1-phenylbenzene

https://huagongshe.com/reaction/1701008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant1-Bromo-2-methyl-4-nitrobenzeneHCID 251672—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Methyl-4-nitro-1-phenylbenzeneHCID 1431741586%

Reaction Steps

According to the method of Preparation 25(a), 2-bromo-5-nitrotoluene (15 gm, 69.4 mmol) was treated with phenyl boronic acid (12.7 gm, 104.1 mmol) under palladium catalysis, using 2M aqueous sodium carbonate as base at reflux in dimethoxyethane for 16 h. After being cooled, the mixture was separated the organic layer was diluted with diethyl ether and washed with water (twice). The organic layer was dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by flash chromatography (gradient elution with hexane to hexane:ethyl acetate 95:5) to give 2-methyl-4-nitro-1-phenylbenzene as a yellow solid (12.7gm, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350907B1
Source datasetuspto-grants-2002_02
ORD IDord-36a908b520c4492abae4c820bdc7ebd4
Source noteuspto-grants-2002_02