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Dimethylformamide → HCID 17989247、化合物

HRID 1443273
ノート
印刷プレビュー

反応式

HRID 1443273 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]#N)=[CH:4][C:3]=1[O:11][CH3:12].[CH3:13]I.[H-].[Na+].C[N:18]([CH3:21])C=O>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:13])([CH3:9])[C:21]#[N:18])=[CH:4][C:3]=1[O:11][CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 179892962-(4-Fluoro-3-methoxyphenyl)acetonitrile

生成物 1

HCID 17989247HCID 17989247、化合物

実験手順

16.67 g (100.93 mmol) of (4-fluoro-3-methoxyphenyl)-acetonitrile is introduced into 158 ml of dimethylformamide with 30.1 g (211.96 mmol) of methyl iodide. At 0° C., 8.50 g (211.96 mmol) of a 55-60% sodium hydride suspension is added in portions. After stirring overnight at room temperature, the reaction mixture is poured onto ice water and then extracted three times with methyl tert-butyl ether. The combined organic extracts are washed with water and with brine. After the solvent is dried and spun off, the residue is chromatographed on silica gel (mobile solvent: ethyl acetate/hexane). 5.11 g (26.2%) of the desired compound and 6.18 g of the monomethyl compound, which is realkylated, are isolated.

後処理

  1. additionthe reaction mixture is poured onto ice water
  2. extractionextracted three times with methyl tert-butyl ether
  3. washThe combined organic extracts are washed with water and with brine
  4. customAfter the solvent is dried
  5. customthe residue is chromatographed on silica gel (mobile solvent: ethyl acetate/hexane)
  6. customare isolated

出典と根拠

ORDレコード
ord-9625087593cc47ac9655c401691ed9ab
出典データセット
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07659297B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート