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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377211Generated: October 30, 2026

4-Nitrobenzoyl chloride → 1,4-Bis(4-(4-nitrobenzoyl)phenylmethyl)benzene

https://huagongshe.com/reaction/1377211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant1,4-DibenzylbenzeneHCID 236047—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventNitrobenzeneHCID 7416—
Product1,4-Bis(4-(4-nitrobenzoyl)phenylmethyl)benzeneHCID 2292051736%

Reaction Steps

In a 2-liter four-necked flask equipped with a stirring device, a thermometer, a condenser and a nitrogen substituting device, 177.4 g of aluminum chloride and 300 milliliters of nitrobenzene were mixed and then 99.54 g of paranitrobenzoyl chloride was introduced with ice cooling to be dissolved. Then, a solution of 46.10 g of 1,4-bis(phenylmethyl)benzene in 100 milliliters of nitrobenzene was added dropwise for 30 minutes. 30 minutes after the end of the dropwise adding, an ice bath was removed and stirring was carried out at room temperature for 40 hours. After the end of the reaction was confirmed by a liquid chromatography, the reaction solution was poured on 1.5 liters of ice, and then extracted with 1.0 liter of chloroform. The solution was filtered through a Celite, washed with a 6N-HCl aqueous solution, an aqueous solution of sodium hydrogencarbonate, brine and water, removed off chloroform by a rotary evaporator, and thereafter removed off nitrobenzene by a steam distillation. By dissolving the solution in chloroform, purifying it with a silica gel column, and recrystallizing it from ethyl acetate, 35.72 g of 1,4-bis(4-(4-nitrobenzoyl)phenylmethyl)benzene was obtained as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663440
Source datasetuspto-grants-1997_09
ORD IDord-05ffe996a9004ff790804ac9fdef6191
Source noteuspto-grants-1997_09