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ChemicalBook CAS DataBase List 1-Phenylnonane

1-Phenylnonane synthesis

14synthesis methods
-

Yield: 88 %Chromat.

Reaction Conditions:

with C20H36BrN3NiO in tetrahydrofuran at 20; for 2 h;Kumada Cross-Coupling;Reagent/catalyst;

Steps:

3.7. Typical Procedure for the Kumada Cross-Coupling Reactions in Table 1
General procedure: A vial was charged with alkyl halide substrate (0.2 mmol) and nickel catalyst (3 mol %), and theinternal standard undecane (0.2 mmol) in THF (3 mL). OctylMgCl (0.24 mmol, 2 M in THF) was thenadded dropwise at room temperature. The resulting solution was stirred at room temperature for 2 h.The reaction mixture was then filtered through a plug of silica gel and analyzed by gaschromatography. The response factor of ethyl undecanoate calibrated to the internal standard was usedto calculate product yields.

References:

Yu, Siqi;Wang, Huan;Sledziewski, Jill E.;Madhira, Venkata N.;Takahashi, Cyrus G.;Leon, Michelle K.;Dudkina, Yulia B.;Budnikova, Yulia H.;Vicic, David A. [Molecules,2014,vol. 19,# 9,p. 13603 - 13613]

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