تفاعل #1583864
ord-2eb4e69c7de2474daa288d4bb6522291
معادلة التفاعل
7-(tert-Butyldimethylsilyloxy)-3-(4-(tert-butyldimethylsilyloxy)phenyl)-4-(4-methoxyphenyl)chroman-4-ol
pTsOH
ethanol
→
3-(4-Hydroxyphenyl)-4-(4-methoxyphenyl)-2H-chromen-7-ol
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىwere combined in a 2-neck 5 L round bottom flask with condenser
- 2درجة الحرارةThe reaction was heated
- 3درجة الحرارةat reflux for 3 hours
- 4تركيزThe solvent was concentrated in vacuo to ˜100 ml
- 5workup.ADDITIONbefore being poured
- 6درجة الحرارةinto chilled
- 7استخلاصThe mixture was then extracted with ethyl acetate
- 8غسيلthe combined organic layers washed with water (3×2 L), brine (1×500 ml)
- 9تجفيفdried over anhydrous magnesium sulphate
- 10ترشيحfiltered
- 11أخرىsolvent removed in vacuo
- 12أخرىto 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.