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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212831Generated: November 1, 2026

2,2'-Dimethylbiphenyl → 6-(4-Methylphenyl)-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/2212831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-DimethylbiphenylHCID 11797—
ReactantTridecaneHCID 12388—
Reactant6-MethoxytetralinHCID 74414—
CatalystHCID 178418751HCID 178418751—
SolventTolueneHCID 1140—
Product6-(4-Methylphenyl)-1,2,3,4-tetrahydronaphthaleneHCID 1114877429%

Reaction Conditions

Temperature110 °C

Reaction Steps

The Grignard reagent (1 M in ether, 5.0 mmol) was placed under vacuum to remove all volatiles. Toluene (5.0 mL) was then added to the Grignard reagent. In a separate reaction flask was placed NiCl2(PPh3)2 (62.0 mg, 0.0948 mmol), tridecane (282 mg, 1.532 mmol, as an internal standard), and 6-methoxy-1,2,3,4-tetrahydronaphthalene (334 mg, 2.059 mmol). The Grignard reagent in toluene was then transferred to this mixture under a nitrogen atmosphere at room temperature. The resulting solution was warmed to 110° C. for 15 hours. A sample was withdrawn and quenched with an aqueous sodium citrate solution (1 M). The aqueous solution was extracted with ethyl acetate. GC analysis of the organic phase showed the presence of 6-(4-methylphenyl)-1,2,3,4-tetrahydronaphthalene (0.598 mmol, 29% yield), bitoluene (0.419 mmol), and 6-methoxy-1,2,3,4-tetrahydronaphthalene (1.043 mmol) in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105467B2
Source datasetuspto-grants-2006_09
ORD IDord-e3da3ca866824d6896d7fec6e2832f2e
Source noteuspto-grants-2006_09