تفاعل #2300016

ord-f815e3f794b34cc7baee9fb28b946f4d

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىIn a reaction flask was placed
  2. 2
    workup.ADDITIONthis solution added to the above catalyst mixture under a nitrogen atmosphere at room temperature
  3. 3
    درجة الحرارةwarmed to 80° C. for 15 hours
  4. 4
    أخرىA sample was withdrawn
  5. 5
    أخرىquenched with an aqueous sodium citrate solution (1 M)
  6. 6
    استخلاصThe resulting aqueous solution was extracted with ethyl acetate

الإجراء التجريبي

In a reaction flask was placed NiCl2(PCy3)2 (49.0 mg, 0.0710 mmol), PCy3 (44.0 mg, 0.157 mmol), tridecane (333 mg, 1.806 mmol, as an internal standard), and 6-methoxy-1,2,3,4-tetrahydronaphthalene (222 mg, 1.368 mmol). The solvent in the Grignard reagent (1 M in ether, 3.70 mmol) was exchanged with i-Pr2O (8.0 mL) and MTBE (2.0 mL) and this solution added to the above catalyst mixture under a nitrogen atmosphere at room temperature. The resulting solution was stirred for several minutes at room temperature and then warmed to 80° C. for 15 hours. A sample was withdrawn and quenched with an aqueous sodium citrate solution (1 M). The resulting 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 (1.030 mmol, 75% yield) and 6-methoxy-1,2,3,4-tetrahydronaphthalene (0.131 mmol) and bitoluene (0.376 mmol) and m-methylphenol (0.220 mmol) in the reaction mixture.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07105467B2uspto-grants-2006_09