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

HRID 529150
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HRID 529150 반응식
[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]
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참가 물질

4

반응물 2

HCID 517165Ammonium AcetateHCID 12840254HCID 12840254, 화합물

생성물 1

HCID 68735644Methyl 2-amino-5-isopropylcyclopent-1-enecarboxylate수율 61%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
50 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-a1ab366b60fc402380f2e367c636d4a0
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346805B2

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