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1-Azabicyclo[2.2.2]octane-4-carbonitrile → Quinuclidin-4-ylmethanamine

HRID 1800815
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HRID 1800815 반응식
[C:1]([C:3]12[CH2:10][CH2:9][N:6]([CH2:7][CH2:8]1)[CH2:5][CH2:4]2)#[N:2].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C(OCC)C>[N:6]12[CH2:9][CH2:10][C:3]([CH2:1][NH2:2])([CH2:8][CH2:7]1)[CH2:4][CH2:5]2
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참가 물질

4

반응물 2

HCID 1412921-Azabicyclo[2.2.2]octane-4-carbonitrileHCID 21226445Aluminium lithium hydride

생성물 1

HCID 22056669Quinuclidin-4-ylmethanamine

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

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온도
23 °C

실험 절차

A solution of 4-cyanoquinuclidine (0.30 g, 2.2 mmol) in diethyl ether (5 mL) was slowly added to a suspension of LAH (0.167 g, 4.41 mmol) in diethyl ether (15 mL) at 0° C. The reaction was stirred at 23° C. for 3 h, then quenched with sodium sulfate decahydrate and stirred for 30 more minutes. Ethyl acetate was then added and, after 30 minutes, celite was added and the suspension was filtered on celite. The filtrate was concentrated to dryness to give an oil (0.310 g, quant.). The compound was used as such for the next reaction. 1H NMR (400 MHz, CDCl3) δ ppm: 1.31-1.40 (6H, m), 2.43 (2H, s), 2.86-2.94 (6H, m).

후처리

  1. customquenched with sodium sulfate decahydrate
  2. stirringstirred for 30 more minutes
  3. additionEthyl acetate was then added and, after 30 minutes
  4. additioncelite was added
  5. filtrationthe suspension was filtered on celite
  6. concentrationThe filtrate was concentrated to dryness
  7. customto give an oil (0.310 g, quant.)
  8. customsuch for the next reaction

출처 및 근거

ORD 기록
ord-54dffeac107847cb858c202ef847b8b3
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08343999B2

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