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

HRID 277022
ノート
印刷プレビュー

反応式

HRID 277022 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide
溶媒
HCID 8028Tetrahydrofuran溶媒2 回

実験手順

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).

後処理

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

出典と根拠

ORDレコード
ord-7134f50ea64a43079d118db321dd3cef
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06355653B1

反応ノート

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