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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193867Generated: November 1, 2026

Cyclohexane → 4-Methyl-3-nitro-1,1'-biphenyl

https://huagongshe.com/reaction/1193867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
Reactant4-Iodo-2-nitrotolueneHCID 170481—
ReactantHCID 178506676HCID 178506676—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4-Methyl-3-nitro-1,1'-biphenylHCID 1290982685%

Reaction Steps

Phenyllithium (10 ml of a 2.0M solution in a 7:3 mixture of cyclohexane and ether, 20 mmol) was added dropwise to zinc chloride (20 ml of a 1.0M solution in ether, 20 mmol) at room temperature. The resulting mixture was stirred for 2 hours, then a solution of 4-iodo-2-nitrotoluene (2.63 g, 10 mmol) in THF (20 ml) and tetrakis(triphenylphosphine)palladium (0.3 g, 0.26 mmol) were added successively. The reaction mixture was stirred for 3 hours then diluted with 0.5M hydrochloric acid (40 ml) and extracted with ether (3×70 ml). The ether extracts were washed with brine, dried, concentrated then purified by column chromatography using petrol (60°-80° C.)-ethyl acetate (9:1) on silica gel to give 4-phenyl-2-nitrotoluene (1.8 g, 85% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04812162
Source datasetuspto-grants-1989_03
ORD IDord-4776b8af320a493f9e61978559b649b3
Source noteuspto-grants-1989_03