تفاعل #90094

ord-36c2b552965943daa97eb9dbe64a655a

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred at 80° C. for 3 hr
  2. 2
    استخلاصthe extraction
  3. 3
    تجفيفThe organic layer was dried over magnesium sulfate
  4. 4
    أخرىThe drying agent was removed by filtration
  5. 5
    أخرىthe residues obtained
  6. 6
    تركيزafter concentration under reduced pressure
  7. 7
    أخرىwere purified by silica gel column chromatography (ethyl acetate/hexane)

الإجراء التجريبي

To the THF (300 ml) solution of 7-methoxy-3,4-dihydro-1H-naphthalen-2-one (Compound A1, 20 g, 0.11 mol), sodium hydride (9.9 g, 3.7 eq.) was added at 0° C. After stirring for 10 min, 1-bromo-2-(2-bromo-ethoxy)-ethane (19 ml, 12 eq.) was added dropwise thereto, and the mixture was stirred at 80° C. for 3 hr. To the reaction solution, saturated aqueous solution of ammonium chloride was added and the extraction was carried out twice with ethyl acetate. The organic layer was dried over magnesium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (white solid, 13 g, 51%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09440922B2uspto-grants-2016_09