Diethyl Ether → 5-(alpha-Hydroxyundecyl)-3-phenylbenzofuran

HRID 262217

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HRID 262217 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]2[O:9][CH:8]=[C:7]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[C:6]=2[CH:16]=1.[Mg].[Cl-].[NH4+].C([O:22][CH2:23][CH3:24])C>O1CCCC1.O>[OH:22][CH:23]([C:2]1[CH:3]=[CH:4][C:5]2[O:9][CH:8]=[C:7]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[C:6]=2[CH:16]=1)[CH2:24][CH2:4][CH2:3][CH2:2][CH2:16][CH2:6][CH2:7][CH2:10][CH2:11][CH3:12]

참가 물질

7

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온도
0 °C

실험 절차

To a solution of 5.5 g. (0.02 mole) of 5-bromo-3-phenylbenzofuran in tetrahydrofuran is added 0.5 g. (0.02 mole) of magnesium, and the mixture is heated at its reflux temperature for three hours. After cooling to 0° C., 3.4 g. of undecyl aldehyde is added. After stirring for 30 minutes at room temperature, the solution is added to ammonium chloride solution. Evaporation provides a residue which is mixed with diethyl ether and water. The ether layer is separated, washed with saturated sodium chloride solution, dried and evaporated. The resulting oil is dissolved in carbon tetrachloride and eluted from a silica gel column with carbon tetrachloride, then with dichloromethane. The later fractions are evaporated to provide 5-(α-hydroxyundecyl)-3-phenylbenzofuran which is dissolved in dichloromethane.

후처리

  1. temperaturereflux temperature for three hours
  2. customEvaporation
  3. customprovides a residue which
  4. customThe ether layer is separated
  5. washwashed with saturated sodium chloride solution
  6. customdried
  7. customevaporated
  8. dissolutionThe resulting oil is dissolved in carbon tetrachloride
  9. washeluted from a silica gel column with carbon tetrachloride
  10. customThe later fractions are evaporated

출처 및 근거

ORD 기록
ord-c49d250a9e154af5b535095b9dcf3100
출처 데이터셋
uspto-grants-1979_05
특허 번호
US04153716

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