تفاعل #1317

ord-8ad41e85bae94573960b3d36e878b3e1

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was refluxed for 6 hours under argon atmosphere
  2. 2
    ترشيحfiltered through celite and
  3. 3
    تركيزconcentrated in vacuo
  4. 4
    أخرىPurification by chromatography (silica, 10% EtOAc-hexane)

الإجراء التجريبي

Employing the above-described procedure for the conversion of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene naphthalene (Compound F) to the dibromonaphthalene derivative (Compond I), 3.5 g (14.6 mmol) of (Compound F), 2.86 g (16.1 mmol) of N-bromosuccinimide and 150 mg (0.62 mmol ) of benzoylperoxide gave crude 4,6-dibromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene (Compound I). To a solution of this crude dibromonaphthalene derivative (Compound I) in 50 ml of THF was added 5.38 g (47.1 mmol) of potassium thioacetate. The mixture was refluxed for 6 hours under argon atmosphere, filtered through celite and concentrated in vacuo. Purification by chromatography (silica, 10% EtOAc-hexane) yielded the title compound as red oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723620uspto-grants-1998_03