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Methanol → 3-(2-Isopropyl-pyridin-4-yl)-acrylonitrile

HRID 277022
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HRID 277022 반응식
[H-].[Na+].[Cl-].[C:4]([CH2:6][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)#[N:5].[CH:26]([C:29]1[CH:34]=[C:33]([CH:35]=O)[CH:32]=[CH:31][N:30]=1)([CH3:28])[CH3:27].CO>O1CCCC1.CN(C)C=O>[CH:26]([C:29]1[CH:34]=[C:33]([CH:35]=[CH:6][C:4]#[N:5])[CH:32]=[CH:31][N:30]=1)([CH3:28])[CH3:27]
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참가 물질

7

반응물 4

HCID 887MethanolHCID 24758Sodium hydrideHCID 197040(Cyanomethyl)triphenylphosphonium chlorideHCID 183135762-Isopropylisonicotinaldehyde

생성물 1

HCID 700882473-(2-Isopropyl-pyridin-4-yl)-acrylonitrile수율 11.5%

시약·촉매·용매 2

HCID 6228
Dimethylformamide
용매
HCID 8028Tetrahydrofuran용매2회

실험 절차

To a suspension of 6.55 g (0.15 mol) sodiumhydride in 220 ml tetrahydrofurane and 220 ml dimethylformamide were added 50.7 g (0.15 mol) (cyanomethyl)triphenylphosphonium chloride. After sirring for 1 hour at room temperature a solution of 22.4 g (0.15 mol) 2-isopropyl-4-pyridinecarboxaldehyde in 50 ml tetrahydrofuran were added and stirring was continued for 15 hours. Then 10 ml methanol were added, the solvents were evaporated and the residue chromatographed on aluminiumoxide with dichloromethane to yield 2.96 g 3-(2-isopropyl-pyridin-4-yl)-acrylonitrile as coorless oil. MS m/e (%): 172 (M+, 100).

후처리

  1. waitwas continued for 15 hours
  2. customthe solvents were evaporated
  3. customthe residue chromatographed on aluminiumoxide with dichloromethane

출처 및 근거

ORD 기록
ord-7134f50ea64a43079d118db321dd3cef
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06355653B1

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