Imidazole → (But-3-yn-1-yloxy)(tert-butyl)dimethylsilane

HRID 462382

反応式

HRID 462382 の反応式
[CH2:1]([OH:5])[CH2:2][C:3]#[CH:4].N1C=CN=C1.[Si:11](Cl)([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12]>CN(C)C=O>[Si:11]([O:5][CH2:1][CH2:2][C:3]#[CH:4])([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12]

参加物

5

実験手順

A mixture of 21 g of 3-butyn-1-ol and 27 g of imidazole in 100 ml of dimethyl formamide was treated with 45 g of t-butyldimethylsilyl chloride in several portions over a one hour period. After stirring under nitrogen for 18 hours the reaction mixture was diluted with 500 ml of ice water. The resulting aqueous solution was extracted with 300 ml of ether and the ethereal solution washed with water and then brine. The ethereal solution was dried over potassium carbonate. Evaporation of the ether and distillation of the residue gave 47.6 g of 3-butyn-1-ol t-butyldimethylsilyl ether, bp 80°-83° C./25 mm.

後処理

  1. extractionThe resulting aqueous solution was extracted with 300 ml of ether
  2. washthe ethereal solution washed with water
  3. dry with materialThe ethereal solution was dried over potassium carbonate
  4. customEvaporation of the ether and distillation of the residue

出典と根拠

ORDレコード
ord-5e65622494834595801ef6ba7857a3f8
出典データセット
uspto-grants-1985_05
特許番号
US04515727

関連ノート

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