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Ammonium Acetate → Methyl 2-amino-5-isopropylcyclopent-1-enecarboxylate

HRID 529150
ノート
印刷プレビュー

反応式

HRID 529150 の反応式
[CH:1]([CH:4]1[CH2:8][CH2:7][C:6](=O)[CH:5]1[C:10]([O:12][CH3:13])=[O:11])([CH3:3])[CH3:2].C([O-])(=O)C.[NH4+:18]>CO>[NH2:18][C:6]1[CH2:7][CH2:8][CH:4]([CH:1]([CH3:3])[CH3:2])[C:5]=1[C:10]([O:12][CH3:13])=[O:11]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 517165Ammonium AcetateHCID 12840254HCID 12840254、化合物

生成物 1

HCID 68735644Methyl 2-amino-5-isopropylcyclopent-1-enecarboxylate収率 61%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
50 °C

実験手順

A solution of methyl 2-isopropyl-5-oxocyclopentanecarboxylate (5.4 g, 29.31 mmol) in MeOH (145 mL) was treated with ammonium acetate (22.59 g, 293.1 mmol), and the mixture was heated to 50° C. for 2 hours and stirred at room temperature overnight. The solvents were removed under reduced pressure, and the crude residue was taken up in DCM and H2O. The combined organics were washed with brine, dried Na2SO4, filtered, and concentrated. The crude residue was purified by column chromatography (5 then 15% EtOAc/Hexane) to yield pure methyl 2-amino-5-isopropylcyclopent-1-enecarboxylate (3.27 g, 61%). LCMS (APCI+) m/z 184.0 [M+H]+; Rt=3.51 min.

後処理

  1. customThe solvents were removed under reduced pressure
  2. washThe combined organics were washed with brine, dried Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe crude residue was purified by column chromatography (5

出典と根拠

ORDレコード
ord-a1ab366b60fc402380f2e367c636d4a0
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09346805B2

反応ノート

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