تفاعل #1583864

ord-2eb4e69c7de2474daa288d4bb6522291

معادلة التفاعل

COc1ccc(C2(O)c3ccc(O[Si](C)(C)C(C)(C)C)cc3OCC2c2ccc(O[Si](C)(C)C(C)(C)C)cc2)cc1
7-(tert-Butyldimethylsilyloxy)-3-(4-(tert-butyldimethylsilyloxy)phenyl)-4-(4-methoxyphenyl)chroman-4-ol
Cc1ccc(S(=O)(=O)O)cc1
pTsOH
CCO
ethanol
COc1ccc(C2=C(c3ccc(O)cc3)COc3cc(O)ccc32)cc1
3-(4-Hydroxyphenyl)-4-(4-methoxyphenyl)-2H-chromen-7-ol

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwere combined in a 2-neck 5 L round bottom flask with condenser
  2. 2
    درجة الحرارةThe reaction was heated
  3. 3
    درجة الحرارةat reflux for 3 hours
  4. 4
    تركيزThe solvent was concentrated in vacuo to ˜100 ml
  5. 5
    workup.ADDITIONbefore being poured
  6. 6
    درجة الحرارةinto chilled
  7. 7
    استخلاصThe mixture was then extracted with ethyl acetate
  8. 8
    غسيلthe combined organic layers washed with water (3×2 L), brine (1×500 ml)
  9. 9
    تجفيفdried over anhydrous magnesium sulphate
  10. 10
    ترشيحfiltered
  11. 11
    أخرىsolvent removed in vacuo
  12. 12
    أخرىto give red/brown oil

الإجراء التجريبي

7-(tert-Butyldimethylsilyloxy)-3-(4-(tert-butyldimethylsilyloxy)phenyl)-4-(4-methoxyphenyl)chroman-4-ol (42 g), pTsOH (435 g), boiling chips and 2.5 L of ethanol were combined in a 2-neck 5 L round bottom flask with condenser attached. The reaction was heated at reflux for 3 hours. The solvent was concentrated in vacuo to ˜100 ml before being poured into chilled, stirred water (700 ml). The mixture was then extracted with ethyl acetate, the combined organic layers washed with water (3×2 L), brine (1×500 ml), dried over anhydrous magnesium sulphate and filtered and solvent removed in vacuo to give red/brown oil. The oil was dissolved in methanol (˜100 ml) and put in freezer overnight.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09198895B2uspto-grants-2015_12