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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377234Generated: November 2, 2026

Hydrochloric Acid → HCID 22919273, compound

https://huagongshe.com/reaction/1377234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantHCID 22919173HCID 22919173—
CatalystFerrous ChlorideHCID 24458—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 22919273HCID 2291927355%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a 10-liters three-necked flask equipped with a stirring device, a thermometer and a nitrogen substituting device, 629 g (3.88 mole) of iron chloride and 1.7 liters of 1,2-dichloroethane were mixed, and 595 g (3.21 mole) of paranitrobenzoyl chloride was introduced with ice cooling to be dissolved. After warming the reaction solution to 80° C., a solution of 391 g (1.34 mole) of 1,1-diphenyl-4-butylcyclohexane in 630 milliliters of 1,2-dichloroethane was added dropwise for 3 hours and 30 minutes. After the dropwise addition was ended, the solution was stirred gently at reflux for 6 hours. After the end of the reaction was confirmed by a liquid chromatography, the reaction solution was poured on 2 liters of ice, and 1 liter of a 4N-HCl aqueous solution was added and then extracted with 1.5 liters of chloroform. The solution was washed with a 6N-HCl aqueous solution, an aqueous solution of sodium hydrogencarbonate, brine and water, and dried with magnesium sulfate. After removing off chloroform by a rotary evaporator, treating with a silica gel column and purifying by recrystallization from ethyl acetate, 435 g of 1,1-bis(4-(4-nitrobenzoyl)phenyl)-4-butylcyclohexane was obtained as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663440
Source datasetuspto-grants-1997_09
ORD IDord-999bc029187d4263a32e5cb89719f816
Source noteuspto-grants-1997_09