Diisopropylamine → Ethyl 1-(3-(tert-butoxy)-3-oxopropanoyl)cyclopropane-1-carboxylate

HRID 342963

反応式

HRID 342963 の反応式
C([Li])CCC.C(NC(C)C)(C)C.[C:13]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])(=[O:15])[CH3:14].[C:21]1([C:29](OCC)=[O:30])([C:24]([O:26][CH2:27][CH3:28])=[O:25])[CH2:23][CH2:22]1.[Cl-].[NH4+]>CCOCC>[CH2:27]([O:26][C:24]([C:21]1([C:29](=[O:30])[CH2:14][C:13]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:23][CH2:22]1)=[O:25])[CH3:28]

参加物

7

反応条件

温度
-78 °C

実験手順

A solution of n-butyllithium (2.5M in hexane, 40 ml) was added dropwise with stirring to a cooled solution of diisopropylamine (10.1 g) in anhydrous ether (100 ml) in an atmosphere of nitrogen, whilst maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 5 hour and a solution of t-butyl acetate (11.6 g) in anhydrous ether (20 ml) was added dropwise, whilst maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 1 hour and a solution of diethyl cyclopropane-1,1-dicarboxylate (18.6 g) in anhydrous ether (20 ml) was added dropwise whilst maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 0.5 hour and the temperature was allowed to rise to room temperature. A saturated solution of ammonium chloride (150 ml) was added cautiously and the layers were separated. The organic extract was washed with water (2×50 ml) hydrochloric acid (2M, 2×50 ml) and water (2×50 ml). The solution was dried (anhydrous sodium sulphate) and filtered. The filtrate was evaporated to dryness and the residue was distilled to give t-butyl 3-(1-ethoxycarbonylcyclopropyl)-3-oxopropionate (11.66 g) as a clear oil bp 89°-90° C./0.5 mmHg.

後処理

  1. temperaturewhilst maintaining the temperature below -70° C
  2. temperaturewhilst maintaining the temperature below -70° C
  3. stirringThe mixture was stirred at -78° C. for 1 hour
  4. temperaturewhilst maintaining the temperature below -70° C
  5. stirringThe mixture was stirred at -78° C. for 0.5 hour
  6. customto rise to room temperature
  7. customthe layers were separated
  8. extractionThe organic extract
  9. washwas washed with water (2×50 ml) hydrochloric acid (2M, 2×50 ml) and water (2×50 ml)
  10. dry with materialThe solution was dried (anhydrous sodium sulphate)
  11. filtrationfiltered
  12. customThe filtrate was evaporated to dryness
  13. distillationthe residue was distilled

出典と根拠

ORDレコード
ord-f9dec02b51f04427a9068269433814fd
出典データセット
uspto-grants-1999_01
特許番号
US05859283

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