تفاعل #61657
ord-75969647c2494c0a89201f948e5b0b16
معادلة التفاعل
المتفاعلات
المذيبات
ظروف التفاعل
المعالجة
- 1ترشيحsuction filtered
- 2غسيلwhile washing repeatedly with diethyl ether
- 3غسيلThe combined organic phases are washed successively with 1 N hydrochloric acid, sodium carbonate solution and sodium chloride solution
- 4workup.DISTILLATIONThe solvent is distilled off
- 5أخرىthe residue is crystallised from ethanol
- 6ترشيحthe solid is filtered off
- 7غسيلwashed 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.