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Methyl iodide → 2-(4-Methoxyphenyl)-2-methylpropan-1-amine

HRID 216133
ノート
印刷プレビュー

反応式

HRID 216133 の反応式
COC1C=CC(CC#N)=CC=1.C([N-]C(C)C)(C)C.[Li+].C1CCCCC1.CI.C(OC1C=CC(C(C)C#N)=CC=1)C.[CH3:41][O:42][C:43]1[CH:48]=[CH:47][C:46]([C:49]([CH3:53])([CH3:52])[C:50]#[N:51])=[CH:45][CH:44]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1.[Cl-].[NH4+]>[CH3:41][O:42][C:43]1[CH:48]=[CH:47][C:46]([C:49]([CH3:53])([CH3:52])[CH2:50][NH2:51])=[CH:45][CH:44]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 7

HCID 6328Methyl iodideHCID 8078CyclohexaneHCID 66031Benzeneacetonitrile, 4-methoxy-HCID 2191662-(4-Methoxyphenyl)-2-methylpropanenitrileHCID 2724682Lithium diisopropylamideHCID 132545222-(4-Ethoxyphenyl)propanenitrileHCID 21226445Aluminium lithium hydride

生成物 1

HCID 35813642-(4-Methoxyphenyl)-2-methylpropan-1-amine収率 33%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒2 回HCID 25517Ammonium Chloride溶媒

実験手順

To a solution of (4-methoxy-phenyl)-acetonitrile [5 g, 34 mmol] in THF (40 mL), is added a 1.5 M solution of lithium diisopropylamide in cyclohexane (36 mL, 54 mmol) at −78° C. After 2 hours at −78° C., methyl iodide (3.4 g, 54 mmol) is added, and the mixture is allowed to warm to room temperature over 3 hours. After additional 12 hours at 20° C., the mixture is diluted with aqueous ammonium chloride solution, and extracted with ethyl acetate. The extracts are dried over magnesium sulfate, filtered and concentrated. The residue is subjected to chromatography on silica gel eluting with 40% EtOAc in heptane to afford a mixture of 2-(4-ethoxy-phenyl)-propionitrile and 2-(4-methoxy-phenyl)-2-methyl-propionitrile. To above mixture (5 g) in THF (20 mL) is add a 2 M solution of lithium aluminum hydride (35 mL, 70 mmol) at 0° C. After 12 hours at 20° C., the mixture is carefully quenched with 10% sodium hydroxide solution, and the white slurry is diluted with ether. The mixture is dried over magnesium sulfate, filtered and concentrated. The residue is subjected to chromatography on silica to afford 2-(4-methoxy-phenyl)-2-methyl-propylamine [2 g, 33%, Intermediate (35)]. MS: 180 (M+H).

後処理

  1. waitAfter additional 12 hours at 20° C.
  2. extractionextracted with ethyl acetate
  3. dry with materialThe extracts are dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customto afford
  7. waitAfter 12 hours at 20° C.
  8. customthe mixture is carefully quenched with 10% sodium hydroxide solution
  9. additionthe white slurry is diluted with ether
  10. dry with materialThe mixture is dried over magnesium sulfate
  11. filtrationfiltered
  12. concentrationconcentrated

出典と根拠

ORDレコード
ord-a2e8851f2c1d4f27b7ceaa176f8c7208
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08193183B2

反応ノート

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