Ammonium Chloride → HCID 22908546、化合物

HRID 1378881ノート

反応式

HRID 1378881 の反応式
FC(F)(F)C1C=CC(CCBr)=CC=1.C(C1CCC(C2CCC(=O)CC2)CC1)CCCC.[NH4+].[Cl-].[F:34][C:35]([F:63])([F:62])[C:36]1[CH:41]=[CH:40][C:39]([CH2:42][CH2:43][C:44]2(O)[CH2:49][CH2:48][CH:47]([CH:50]3[CH2:55][CH2:54][CH:53]([CH2:56][CH2:57][CH2:58][CH2:59][CH3:60])[CH2:52][CH2:51]3)[CH2:46][CH2:45]2)=[CH:38][CH:37]=1>C1(C)C=CC=CC=1.C(OCC)C>[F:34][C:35]([F:62])([F:63])[C:36]1[CH:37]=[CH:38][C:39]([CH2:42][CH2:43][C:44]2[CH2:49][CH2:48][CH:47]([CH:50]3[CH2:55][CH2:54][CH:53]([CH2:56][CH2:57][CH2:58][CH2:59][CH3:60])[CH2:52][CH2:51]3)[CH2:46][CH:45]=2)=[CH:40][CH:41]=1

参加物

7

反応条件

温度
60 °C

実験手順

A mixture of dry Mg (0.77 g, 0.032 mol), 2-(4-tri-fluoromethylphenyl)ethyl bromide (8.0 g, 0.032 mol) obtained at the second step and diethyl ether (40 ml) was heated at 60° C. for one hour in a sealed tube reactor to obtain a gray, uniform solution, followed by adding this solution to a diethyl ether (30 ml) solution of 4-(4-pentylcyclohexyl)cyclohexanone (7.9 g, 0.032 mol), stirring the mixture at room temperature for 3 hours, feeding the resulting reaction substance into a saturated aqueous solution of NH4Cl, twice extracting with ethyl acetate (50 ml), washing the resulting organic layer, with an aqueous solution of NaCl, drying over anhydrous MgSO4, removing anhydrous MgSO4, distilling off the solvent under reduced pressure, to obtain pale yellow, oily 1-(2-(4-trifluoromethylphenyl)ethyl)-4-(4-pentylcyclohexyl)cyclohexanol (11.4 g), adding thereto toluene (50 ml) and Amberlyst (0.7 g), heating the mixture under reflux for one hour, while removing water formed by the reaction, allowing the resulting substance to cool, feeding it to a saturated aqueous solution of NH4Cl (100 ml), twice washing the resulting separated organic layer with water, drying over anhydrous magnesium sulfate, filtering off the anhydrous MgSO4, distilling off the solvent under reduced pressure, subjecting the resulting residue to column chromatography (silica gel, eluent: heptane) and twice recrystallizing from ethanol (20 ml), to obtain 1-(2-(4-trifluoromethylphenyl)ethyl)-4-(4-pentylcyclohexyl)cyclohexene (4.1 g). Yield: 32%.

後処理

  1. customto obtain a gray, uniform solution
  2. extractiontwice extracting with ethyl acetate (50 ml)
  3. washwashing the resulting organic layer
  4. dry with materialwith an aqueous solution of NaCl, drying over anhydrous MgSO4
  5. customremoving anhydrous MgSO4
  6. distillationdistilling off the solvent under reduced pressure
  7. customto obtain pale yellow
  8. temperatureunder reflux for one hour
  9. customwhile removing water
  10. customformed by the reaction
  11. temperatureto cool
  12. washtwice washing the resulting
  13. customseparated organic layer with water
  14. dry with materialdrying over anhydrous magnesium sulfate
  15. filtrationfiltering off the anhydrous MgSO4
  16. distillationdistilling off the solvent under reduced pressure
  17. customtwice recrystallizing from ethanol (20 ml)

出典と根拠

ORDレコード
ord-44212b0d9712468c842bfc468e2a3624
出典データセット
uspto-grants-1997_09
特許番号
US05670085

反応ノート

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