تفاعل #320785

ord-d08210b56f49494ba7016092a97b7f32

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONUpon completion of addition
  2. 2
    استخلاصThe mixture is then extracted with two 200 mL portions of diethyl ether
  3. 3
    غسيلThe combined extracts are washed with two 100 mL portions of an aqueous 10% lithium chloride solution
  4. 4
    تجفيفThe organic layer is dried with magnesium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    تركيزThe filtrate is concentrated under reduced pressure

الإجراء التجريبي

A stirred solution of 10.0 grams (0.061 mole) of 7-amino-2,3-dihydro-2,2-dimethylbenzofuran in 150 mL of N,N-dimethylformamide is cooled in an ice-water bath, and a solution of 10.9 grams (0.061 mole) of N-bromosuccinimide in 50 mL of N,N-dimethylformamide is added in one portion. Upon completion of addition, the reaction mixture is maintained in the ice-water bath for about one hour After this time the reaction mixture is poured into about 600 mL of water. The mixture is then extracted with two 200 mL portions of diethyl ether. The combined extracts are washed with two 100 mL portions of an aqueous 10% lithium chloride solution. The organic layer is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 12.3 grams of 7-amino-4-bromo-2,3-dihydro-2,2-dimethylbenzofuran. The NMR spectrum is consistent with the proposed structure.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05593998uspto-grants-1997_01