Water → Ethyl 4-amino-2-methylcyclohexane-1-carboxylate

HRID 1914637

反応式

HRID 1914637 の反応式
[CH3:1][C:2]1[CH:3]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:4][CH2:5][C:6](=O)[CH:7]=1.O.C([O-])=O.[NH4+:18]>CO.[Pd]>[NH2:18][CH:6]1[CH2:5][CH2:4][CH:3]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:2]([CH3:1])[CH2:7]1

参加物

6

反応物 3

HCID 962WaterHCID 790204-Carbethoxy-3-methyl-2-cyclohexen-1-oneHCID 2723923Ammonium formate

生成物 1

HCID 57465891Ethyl 4-amino-2-methylcyclohexane-1-carboxylate

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

Ethyl 2-methyl-4-oxocyclohex-2-enecarboxylate (2.0 g, 10.98 mmol) is dissolved in MeOH (40 ml) and water (4.0 ml) to give a yellow solution. Ammonium formate (8.31 g, 132 mmol) is added and stirred at RT until the suspension dissolves to form a solution. Palladium on carbon (0.117 g, 1.098 mmol) is added and the reaction mixture is stirred at 70° C. for 1 hour. The mixture is filtered through Celite® (filter material) and washed with MeOH. The filtrate is concentrated in vacuo and the residue is partitioned between EtOAc and water. The aqueous portion is diluted with sat. sodium bicarbonate and washed with EtOAc. The pH is adjusted to pH14 using 1M NaOH and the aqueous is extracted with EtOAc. The combined organic extracts are dried MgSO4, filtered and concentrated in vacuo to afford the title compound; [MH]+186.24.

後処理

  1. dissolutiondissolves
  2. customto form a solution
  3. stirringthe reaction mixture is stirred at 70° C. for 1 hour
  4. filtrationThe mixture is filtered through Celite® (filter material)
  5. washwashed with MeOH
  6. concentrationThe filtrate is concentrated in vacuo
  7. customthe residue is partitioned between EtOAc and water
  8. additionThe aqueous portion is diluted with sat. sodium bicarbonate
  9. washwashed with EtOAc
  10. extractionthe aqueous is extracted with EtOAc
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-e85f1763d17a44ada6759b3b8e879d01
出典データセット
uspto-grants-2013_12
特許番号
US08614213B2

関連ノート

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