Triethylene Glycol → 4-(4-Ethylphenoxy)piperidine

HRID 463325ノート

反応式

HRID 463325 の反応式
[C:1]([C:4]1[CH:16]=[CH:15][C:7]([O:8][CH:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)=[CH:6][CH:5]=1)(=O)[CH3:2].C([O-])(=O)C([O-])=O.[OH-].[K+].O.NN.C(O)COCCOCCO>>[CH2:1]([C:4]1[CH:16]=[CH:15][C:7]([O:8][CH:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)=[CH:6][CH:5]=1)[CH3:2]

参加物

6

実験手順

A solution of 4-(4-acetylphenoxy)piperidine (liberated from 15.0 g, 48.5 mmol, of the oxalate), 7.45 g of potassium hydroxide, 5.39 ml of 85% hydrazine hydrate and 54 ml of triethyleneglycol was stirred at reflux for 1 hour. The mixture was then cooled to room temperature and the flask fitted with a distillation apparatus. The temperature was then raised to 190°-195° and water removed by distillation. The mixture was stirred at 190°-195° for 3 hours and the mixture allowed to cool to room temperature. The mixture was diluted with water, extracted twice with ether and with 1N HCl, made basic with saturated sodium carbonate, extracted with ether and dried over potassium carbonate. Filtration followed by evaporation of the solvent provided an oil. Kugelrohr distillation at 114°-116°/1 mm provided 3.84 g (18.7 mmol, 38.6%) of 4-(4-ethylphenoxy)piperidine, m.p. 37-41.

後処理

  1. temperatureat reflux for 1 hour
  2. customthe flask fitted with a distillation apparatus
  3. temperatureThe temperature was then raised to 190°-195°
  4. customwater removed by distillation
  5. stirringThe mixture was stirred at 190°-195° for 3 hours
  6. temperatureto cool to room temperature
  7. additionThe mixture was diluted with water
  8. extractionextracted twice with ether and with 1N HCl
  9. extractionextracted with ether
  10. dry with materialdried over potassium carbonate
  11. filtrationFiltration
  12. customfollowed by evaporation of the solvent
  13. customprovided an oil
  14. distillationKugelrohr distillation at 114°-116°/1 mm

出典と根拠

ORDレコード
ord-252253e7c675432f96f0686e96717777
出典データセット
uspto-grants-1985_05
特許番号
US04518713

反応ノート

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