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Methyl iodide → HCID 67244819、化合物

HRID 2425060
ノート
印刷プレビュー

反応式

HRID 2425060 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:7][OH:8])[O:5][CH:6]=1.[H-].[Na+].I[CH3:12]>CS(C)=O>[Br:1][C:2]1[CH:3]=[C:4]([CH2:7][O:8][CH3:12])[O:5][CH:6]=1
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 12289784(4-Bromofuran-2-yl)methanol

生成物 1

HCID 67244819HCID 67244819、化合物

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

To a solution of 1.062 g (4-bromo-furan-2-yl)-methanol in 10 ml dimethylsulfoxide was added 0.288 of sodium hydride (55%) in oil and 0.56 ml of iodomethane and the reaction mixtures was stirred at room temperature for 18 h. The reaction mixture was partitioned between ethyl acetate and water. The phases were separated; the organic phase was washed with citric acid (10% in water), water, satd. sodiumbicarbonate and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by chromatography on silica gel to yield 0.731 g of a light yellow liquid.

後処理

  1. customthe reaction mixtures
  2. customThe reaction mixture was partitioned between ethyl acetate and water
  3. customThe phases were separated
  4. washthe organic phase was washed with citric acid (10% in water), water
  5. dry with materialsodiumbicarbonate and brine, dried over magnesium sulfate
  6. customevaporated under reduced pressure
  7. customThe residue was purified by chromatography on silica gel

出典と根拠

ORDレコード
ord-9a686c44a52e49b2a255e32bf1cbe324
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07964633B2

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