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Ethylene Glycol → 2-(tert-Butyl(dimethyl)silyl)oxyethanol

HRID 218992
ノート
印刷プレビュー

反応式

HRID 218992 の反応式
[CH2:1]([OH:4])[CH2:2][OH:3].[H-].[Na+].[Si:7](Cl)([C:10]([CH3:13])([CH3:12])[CH3:11])([CH3:9])[CH3:8].P([O-])([O-])([O-])=O>C1COCC1>[Si:7]([O:3][CH2:2][CH2:1][OH:4])([C:10]([CH3:13])([CH3:12])[CH3:11])([CH3:9])[CH3:8]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 174Ethylene GlycolHCID 1061PhosphateHCID 24758Sodium hydrideHCID 28928tert-Butyldimethylsilyl chloride

生成物 1

HCID 111376652-(tert-Butyl(dimethyl)silyl)oxyethanol収率 67.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
20 °C

実験手順

Ethylene glycol (2.00 g) in anhydrous THF (60 ml) under nitrogen was treated portionwise with sodium hydride (60% dispersion in mineral oil, 1.29 g) and the mixture stirred at 20° C. for 45 min. Tert-butyl dimethylsilyl chloride (4.86 g) was added and the mixture stirred at 20° C. for 45 min. Phosphate buffer (60 ml, pH6.5) was added and the mixture stirred for 20 min before extracting with ether (60 ml). The organic layer was then washed with water (60 ml) and brine (60 ml), before drying over Na2SO4, filtering, and removing the solvent in vacuo. This was purified by flash chromatography on silica. Elution with 1:4 EtOAc/cyclohexane followed by solvent evaporation in vacuo gave the title compound (3.82 g). TSP+ve 194 MNH4+.

後処理

  1. stirringthe mixture stirred at 20° C. for 45 min
  2. stirringthe mixture stirred for 20 min
  3. extractionbefore extracting with ether (60 ml)
  4. washThe organic layer was then washed with water (60 ml) and brine (60 ml)
  5. dry with materialbefore drying over Na2SO4
  6. filtrationfiltering
  7. customremoving the solvent in vacuo
  8. customThis was purified by flash chromatography on silica
  9. washElution with 1:4 EtOAc/cyclohexane
  10. customfollowed by solvent evaporation in vacuo

出典と根拠

ORDレコード
ord-b4b6a62c649948de851411454b33d47f
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08198483B2

反応ノート

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