تفاعل #161520

ord-7efadc1324c640deab996a67ddde556b

معادلة التفاعل

CCC1(CC)CO1
2,2-Diethyloxirane
Oc1cccc(Br)c1
3-bromophenol
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CCC(O)(CC)COc1cccc(Br)c1
3-((3-bromophenoxy)methyl)pentan-3-ol

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
120°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصCrude product was extracted from water with diethyl ether
  2. 2
    غسيلThe combined organic was washed with brine
  3. 3
    تجفيفdried over Na2SO4
  4. 4
    ترشيحfiltered
  5. 5
    تركيزconcentrated under reduced vacuum
  6. 6
    أخرىPurification by flash chromatography (0-20% EtOAc/hexanes gradient)

الإجراء التجريبي

2,2-Diethyloxirane (6.5 g of a 60% crude, 40 mmol), 3-bromophenol (5.7 g, 33 mmol), and cesium carbonate (12.0 g, 37 mmol) were combined in anhydrous DMSO (20 mL) in a sealed pressure tube and the reaction was stirred and heated at 120° C. for 2 d. Crude product was extracted from water with diethyl ether. The combined organic was washed with brine, dried over Na2SO4, filtered and concentrated under reduced vacuum. Purification by flash chromatography (0-20% EtOAc/hexanes gradient) gave 3-((3-bromophenoxy)methyl)pentan-3-ol as a colorless oil. Yield (7.1 g, 79%): NMR (400 MHz, CDCl3) δ 7.19 (t, J=8.0 Hz, 1H), 7.05-7.12 (m, 2H), 6.90-6.94 (m, 1H), 4.31 (s, 1H), 3.71 (s, 2H), 1.41-1.55 (m, 4H), 0.80 (t, J=7.6 Hz, 6H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08829244B2uspto-grants-2014_09