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Cyclopentanone → 1-(Dimethylamino)cyclopentanecarbonitrile

HRID 20783
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반응식

HRID 20783 반응식
Cl.[CH3:2][NH:3][CH3:4].[C:5]1(=O)[CH2:9][CH2:8][CH2:7][CH2:6]1.[C-:11]#[N:12].[K+]>O>[CH3:2][N:3]([CH3:4])[C:5]1([C:11]#[N:12])[CH2:9][CH2:8][CH2:7][CH2:6]1
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참가 물질

5

반응물 3

HCID 8452CyclopentanoneHCID 9032Potassium CyanideHCID 10473Dimethylamine, hydrochloride

생성물 1

HCID 107730491-(Dimethylamino)cyclopentanecarbonitrile수율 90.4%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a suspension of dimethylamine hydrochloride (8.15 g; 0.1 mol) in cyclopentanone (8.4 g; 0.1 mol) cooled (ice bath) was added dropwise a solution of potassium cyanide (6.5 g; 0.1 mol) in water (50 ml) over 10 min. After vigorous stirring at room temperature for 18 h, the crude reaction mixture was extracted three times with diethyl ether (3×200 ml) and the combined extracts washed twice with water (2×50 ml), dried (Na2SO4), and evaporated to afford the title product as a pale yellow oil (12.5 g) which was used without further purification. 1H NMR (CDCl3) δ: 1.7-2.0 (6H, m), 2.15-2.3 (2H, m), 3.3 (6H, s). Mass Spectrum (Electrospray LC/MS): Found 112 (MH+−HCN). C8H14N2 requires 138.

후처리

  1. temperaturecooled (ice bath)
  2. customthe crude reaction mixture
  3. extractionwas extracted three times with diethyl ether (3×200 ml)
  4. washthe combined extracts washed twice with water (2×50 ml)
  5. dry with materialdried (Na2SO4)
  6. customevaporated

출처 및 근거

ORD 기록
ord-8614649301fe4c808a29ae62cc1fd84c
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07745642B2

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