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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36721Generated: October 23, 2026

Ethanol → 4-Nitro-1,1'-biphenyl

https://huagongshe.com/en/reaction/36721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
ReactantPhenylboronic AcidHCID 66827—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthyl AcetateHCID 8857—
Solvent1,1-DimethoxyethaneHCID 10795—
Product4-Nitro-1,1'-biphenylHCID 7114127.3%

Reaction Steps

12.50 g (61.9 mmol) of 1-bromo-4-nitrobenzene were added to 358 mg, (310 μmol, 0.5 mole %) of tetrakis (triphenyl-phosphine) palladium in 200 ml of dimethoxy-ethane. After stirring for 10 minutes, 11.3 g (92.8 mmol) of phenylboronic acid and 100 ml of ethanol were added. After a further 10 minutes, 263 ml, (526 mmol, 8.5 equiv) of 2M aqueous sodium carbonate were added and the suspension was heated at reflux for 20 minutes, then allowed to cool to room temperature. The mixture was taken into 250 ml of EtOAc and 200 ml of H2. The aqueous layer was extracted with 200 ml of EtOAc and the combined organics were washed twice with 250 ml of water and 100 ml of brine, dried over MgSO4, filtered and evaporated to obtain 15.7 g of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05416112
Source datasetuspto-grants-1995_05
ORD IDord-cde7e681c41a47928ae7eb2e213796e5
Source noteuspto-grants-1995_05