تفاعل #61657

ord-75969647c2494c0a89201f948e5b0b16

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحsuction filtered
  2. 2
    غسيلwhile washing repeatedly with diethyl ether
  3. 3
    غسيلThe combined organic phases are washed successively with 1 N hydrochloric acid, sodium carbonate solution and sodium chloride solution
  4. 4
    workup.DISTILLATIONThe solvent is distilled off
  5. 5
    أخرىthe residue is crystallised from ethanol
  6. 6
    ترشيحthe solid is filtered off
  7. 7
    غسيلwashed with ethanol

الإجراء التجريبي

5.88 g (6.42 mmol) tris-(dibenzylideneacetone)-dipalladium, 3.50 g (12.01 mmol) tri-tert-butylphosphonium tetrafluoroborate, 81.2 mL (371 mmol) dicyclohexylmethylamine, 105.8 g (286 mmol) tetrabutylammonium iodide and 32.6 mL (362 mmol) methylacrylate are added to a solution of 100 g (238 mmol) 2-acetyl-4-benzyloxy-6-nitro-phenyl trifluoromethanesulphonate in 360 mL dioxane. The reaction mixture is stirred for 2 hours at 80° C. under a nitrogen atmosphere in the presence of 100 g molecular sieve 4A and then combined with 2 L diethyl ether and 500 g silica gel. After 10 minutes the silica gel is suction filtered, while washing repeatedly with diethyl ether. The combined organic phases are washed successively with 1 N hydrochloric acid, sodium carbonate solution and sodium chloride solution. The solvent is distilled off, the residue is crystallised from ethanol and the solid is filtered off and washed with ethanol.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07429583B2uspto-grants-2008_09