تفاعل #43922
ord-d7ee921b6bcb4e169dc24c8ef8291e54
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةcooled
- 2استخلاصextracted with ethyl acetate
- 3غسيلThe extract was washed with saturated brine
- 4تجفيفdried over anhydrous magnesium sulfate
- 5تركيزconcentrated under reduced pressure
- 6أخرىThe residue was purified by silica gel column chromatography (ethyl acetate:hexane=40:60-80:20)
- 7أخرىthe obtained crystals were recrystallized from heptane-ethyl acetate
الإجراء التجريبي
A solution of 3′-fluoro-2′,6′-dimethyl-4′-[3-(methylsulfonyl)propoxy]biphenyl-3-carbaldehyde (2.77 g, 8.00 mmol) in a mixed solvent of methanol (10 mL) and tetrahydrofuran (20 mL) was ice-cooled, sodium borohydride (90%, 0.336 g, 8.00 mmol) was added, and the mixture was stirred for 8 hr under nitrogen atmosphere. The reaction mixture was treated with diluted hydrochloric acid, and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=40:60-80:20), and the obtained crystals were recrystallized from heptane-ethyl acetate to give the title compound (2.75 g, yield 94%) as colorless crystals.