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Trimethylsilyl cyanide → 2-Amino-1-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)ethan-1-ol

HRID 1033017
ノート
印刷プレビュー

反応式

HRID 1033017 の反応式
[CH3:1][O:2][C:3]1[N:10]=[C:9]([CH3:11])[C:8]([CH2:12][CH3:13])=[CH:7][C:4]=1[CH:5]=[O:6].C[Si]([C:18]#[N:19])(C)C.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C(OCC)C.[I-].[Zn+2].[I-]>[CH3:1][O:2][C:3]1[C:4]([CH:5]([OH:6])[CH2:18][NH2:19])=[CH:7][C:8]([CH2:12][CH3:13])=[C:9]([CH3:11])[N:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 82115Trimethylsilyl cyanideHCID 102616792-Methoxy-5-ethyl-6-methylnicotinaldehydeHCID 21226445Aluminium lithium hydride

生成物 1

HCID 103307592-Amino-1-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)ethan-1-ol

試薬・触媒・溶媒 2

HCID 9883512zinc(II)iodide触媒HCID 3283
Diethyl Ether
溶媒
2 回

実験手順

A mixture of 2-methoxy-5-ethyl-6-methylnicotinaldehyde (1.05 g, 5.86 mmol) and trimethylsilyl cyanide (0.85 mL, 6.37 mmol) containing zinc iodide (10 mg) was stirred, under a nitrogen atmosphere, at ambient temperature for two hours. This liquid was diluted with anhydrous diethyl ether, filtered and then added dropwise to a suspension of lithium aluminum hydride (225 mg, 5.9 mmol) in diethyl ether (15 mL) under nitrogen. After two hours the reaction was quenched with saturated aqueous sodium sulfate, diluted with methylene chloride, filtered and the solvents evaporated to give a semi-solid. This residue was triturated with cold diethyl ether and the crystalline product was collected by filtration to yield 346 mg (28%).

後処理

  1. filtrationfiltered
  2. customAfter two hours the reaction was quenched with saturated aqueous sodium sulfate
  3. additiondiluted with methylene chloride
  4. filtrationfiltered
  5. customthe solvents evaporated
  6. customto give a semi-solid
  7. customThis residue was triturated with cold diethyl ether
  8. filtrationthe crystalline product was collected by filtration
  9. customto yield 346 mg (28%)

出典と根拠

ORDレコード
ord-989f814f22c349e0b0631f4de664ba38
出典データセット
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05308854

反応ノート

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