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Methyl iodide → HCID 60026352、化合物

HRID 400646
ノート
印刷プレビュー

反応式

HRID 400646 の反応式
[CH3:1][C:2]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)([CH2:5][CH:6]=[CH2:7])[CH2:3][OH:4].[H-].[Na+].[CH3:16]I>CN(C=O)C>[CH3:16][O:4][CH2:3][C:2]([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)([CH3:1])[CH2:5][CH:6]=[CH2:7]
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 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 3019061beta-Allyl-beta-methylphenethyl alcohol

生成物 1

HCID 60026352HCID 60026352、化合物収率 98.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 2-methyl-2-phenylpent-4-en-1-ol (3.2 g, 18.15 mmol) in 17 mL of DMF was added sodium hydride (1.25 g, 31.25 mmol, 60% in mineral oil). The mixture was stirred until foaming ceased and then methyl iodide (6 mL, 96 mmol) was added. After 2 hours, the mixture was quenched with 50 mL of saturated aqueous ammonium chloride solution and extracted with three 50 mL portions of ethyl acetate. The combined organic layers were washed with 30 mL of saturated aqueous ammonium chloride solution, five 25 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 3.4 g (98.4% yield) of (1-methoxymethyl-1-methylbut-3-enyl)benzene which was used without further purification.

後処理

  1. customthe mixture was quenched with 50 mL of saturated aqueous ammonium chloride solution
  2. extractionextracted with three 50 mL portions of ethyl acetate
  3. washThe combined organic layers were washed with 30 mL of saturated aqueous ammonium chloride solution, five 25 mL portions of brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-1759b24fe55b4439a0f5b7ed36b2830d
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08741897B2

反応ノート

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