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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026774Generated: November 2, 2026

1-Chloro-2,6-dinitrobenzene → 1,1'-Biphenyl, 2,2',6,6'-tetranitro-

https://huagongshe.com/reaction/1026774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2,6-dinitrobenzeneHCID 11814—
ReactantHCID 131731402HCID 131731402—
CatalystCopperHCID 23978—
SolventEthyl AcetateHCID 8857—
Product1,1'-Biphenyl, 2,2',6,6'-tetranitro-HCID 16494663.9%

Reaction Conditions

Temperature180 °C

Reaction Steps

Pre-treatment of copper powder: The copper powder (5.0 g, 78 mmol) was weighted and added into to a 20 mL of 2% iodine/acetone solution. The mixture was stirred for 10 minutes, and filtered in vacuum. The resultant was added into 20 mL of mixed solution of acetone:hydrochloric acid=1:1. The resultant mixture was stirred for 10 minutes, filtered, and dried in vacuum. The 2,6-dinitrochlorobenzene (3.04 g, 15 mmol) and copper powder (2.88 g, 45 mmol) were added into a 250 mL round flask, and were mixed homogeneously. Under the protection of nitrogen gas, the mixture was heated at 180° C. under stirring in an oil bath for two hours. Upon completion of the reaction, the solid in the flask was grounded, and dissolved in 20 mL of ethyl acetate. The solid was filtered off, and the filtration was collected and rotary evaporated. The residue was recrystallized from a mixed solution of ethyl acetate: petroleum ether=10:1, to precipitate a pale yellow needle-like crystal. The crystal was filtered in vacuum, to afford the product in a yield of 63.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729303B2
Source datasetuspto-grants-2014_05
ORD IDord-a27e0a76f8424bdbb827152356f76291
Source noteuspto-grants-2014_05