تفاعل #4976

ord-524d531152204c2e8e6ceed8643f94a1

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGslowly with stirring
  2. 2
    workup.STIRRINGto stir as above for 72 hours
  3. 3
    ترشيحAfter this time the reaction mixture is filtered through a pad of diatomaceous earth
  4. 4
    غسيلThe precipitate is washed with chloroform (5×10 mL)
  5. 5
    استخلاصthe combined organic filtrates are extracted with 1M aqueous HCl (1×75 mL), saturated aqueous sodium bicarbonate solution (1×75 mL), 1M sodium thiosulfate (1×75 mL), and water (1×75 mL)
  6. 6
    تجفيفThe organic layer is dried over anhydrous sodium sulfate
  7. 7
    ترشيحfiltered
  8. 8
    أخرىevaporated under reduced pressure
  9. 9
    تجفيفdried in vacuo to an orange-brown powder (440 mg)

الإجراء التجريبي

A mixture of 7-hydroxy-2-octadecyl-3H-phenoxazine-3-one ("octadecylresorufin) (220 mg, 0.47 mmole), powdered, activated 4Å molecular sieves (0.5 g), sym-collidine (125 μL, 0.95 mmole), and silver carbonate (155 mg, 0.56 mmole) in dry dichloromethane (20 mL) is allowed to stir at room temperature, under an atmosphere of dry nitrogen gas, in the dark for 1 hour. To this mixture is added 1-bromo-2,3,4,6-tetra-O-acetyl-α-D-galactopyranoside (389 mg, 0.95 mmole), slowly with stirring, and the resulting heterogenous solution allowed to stir as above for 72 hours. After this time the reaction mixture is filtered through a pad of diatomaceous earth. The precipitate is washed with chloroform (5×10 mL) and the combined organic filtrates are extracted with 1M aqueous HCl (1×75 mL), saturated aqueous sodium bicarbonate solution (1×75 mL), 1M sodium thiosulfate (1×75 mL), and water (1×75 mL). The organic layer is dried over anhydrous sodium sulfate, filtered, evaporated under reduced pressure, and dried in vacuo to an orange-brown powder (440 mg). An analytical sample of the title compound can be isolated by preparative t.l.c. (20×20 cm SiO2 plate; eluent=9:1 chloroform:ethylacetate) with the bright-orange product eluting at the highest Rf (0.44), (50 mg from 200 mg applied).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05242805uspto-grants-1993_09