تفاعل #50640

ord-747befdf939047769ae78720d23bd309

معادلة التفاعل

O=c1ccc2cc(O)c(OCc3ccccc3)cc2o1
6-hydroxy-7-phenylmethoxy-2H-1-benzopyran-2-one
CC(C)Br
isopropylbromide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
[I-].[K+]
potassium iodide
CC(C)Oc1cc2ccc(=O)oc2cc1O
7-hydroxy-6-(1-methylethoxy)-2H-1-benzopyran-2-one

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحAfter filtration the filtrate
  2. 2
    أخرىis evaporated
  3. 3
    أخرىthe product recrystallized from isopropanol, yield: 57.7 g (100%) 6-(1-methyl-ethoxy)-7-(phenylmethoxy)-2H-1-benzopyran-2-one
  4. 4
    أخرىThis is followed by evaporation and purification
  5. 5
    أخرى24.65 g (69%), fusion point 121°-122° C. (from isopropanol)

الإجراء التجريبي

50.0 g (186 mmol) 6-hydroxy-7-phenylmethoxy-2H-1-benzopyran-2-one, 36.3 ml (387 mmol) isopropylbromide, 51.5 g (373 mmol) potassium carbonate and 5.0 g potassium iodide are agitated in 500 ml DMF for 14 h at 80° C. After filtration the filtrate is evaporated and the product recrystallized from isopropanol, yield: 57.7 g (100%) 6-(1-methyl-ethoxy)-7-(phenylmethoxy)-2H-1-benzopyran-2-one. Of this 50.0 g (161 mmol) are agitated in 100 ml of glacial acetic acid and 90 ml concentrated hydrochloric acid for 2.5 h at 70° C. This is followed by evaporation and purification using column chromatography on silica gel (eluent: chloroform and methanol 98/2 H 95/5): 24.65 g (69%), fusion point 121°-122° C. (from isopropanol).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05428038uspto-grants-1995_06