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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377231Generated: October 31, 2026

Diphenylmethane → HCID 15123923, compound

https://huagongshe.com/reaction/1377231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylmethaneHCID 7580—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 15123923HCID 1512392362.6%

Reaction Conditions

Temperature47 °C

Reaction Steps

In a 10-liters three-necked flask equipped with a stirring device, a thermometer and a nitrogen substituting device, 1300 g (9.75 mole) of aluminum chloride and 4.2 liters of 1,2-dichloroethane were mixed, and 1323 g (7.13 mole) of paranitrobenzoyl chloride was introduced with ice cooling to be dissolved. After warming the reaction solution to 47° C., a solution of 500 g (2.97 mole) of diphenylmethane in 500 milliliters of 1,2-dichloroethane was added dropwise for 3 hours and 30 minutes. After the dropwise addition was ended, the solution was stirred at 50° C. for 4 hours. After the end of the reaction was confirmed by a liquid chromatography, the reaction solution was poured in 7 liters of ice water, and then extracted with 7 liters of chloroform. The solution was washed with a 6N-HCl aqueous solution, an aqueous solution of sodium hydrogencarbonate, brine and water, and then dried with magnesium sulfate. After removing off chloroform by a rotary evaporator, filtration was carried out when crystals being deposited sufficiently. Filtered substances were treated with a silica gel column and recrystallized from chloroform/ethyl acetate, to obtain 867 g of 1,1-bis(4-(4-nitrobenzoyl)phenyl)methane as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663440
Source datasetuspto-grants-1997_09
ORD IDord-1d9ed6d384ce40ebaca32fa75b06f7eb
Source noteuspto-grants-1997_09