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

HRID 21420
ノート
印刷プレビュー

反応式

HRID 21420 の反応式
[Si:1](Cl)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[CH2:9]([OH:12])[CH2:10][OH:11].C(N(CC)CC)C>ClCCl.CN(C)C1C=CN=CC=1>[Si:1]([O:11][CH2:10][CH2:9][OH:12])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 174Ethylene GlycolHCID 8471TriethylamineHCID 28928tert-Butyldimethylsilyl chloride

生成物 1

HCID 111376652-(tert-Butyl(dimethyl)silyl)oxyethanol

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane溶媒2 回
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

実験手順

tert-Butyldimethylsilylchloride (100 g, 0.66M) in dry dichloromethane (70 ml) was added, drop-wise, to a stirred mixture of distilled ethylene glycol (205.6 g, 3.31M), dry dichloromethane (200 ml), triethylamine (120 ml, 0.86M) and 4-dimethylaminopyridine (8 g, 0.066M) at 0° C. under a nitrogen atmosphere. After the addition the mixture was allowed to warm to ambient temperature and was stirred for a further 3 hours. The mixture was then filtered and the filtrate washed with dilute sodium bicarbonate solution, brine, dried over magnesium sulphate, filtered and then evaporated in vacuo to give a pale yellow oil.

後処理

  1. additionAfter the addition the mixture
  2. filtrationThe mixture was then filtered
  3. washthe filtrate washed with dilute sodium bicarbonate solution, brine
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customto give a pale yellow oil

出典と根拠

ORDレコード
ord-71d56f7843c34c92b8e9452de76d3000
出典データセット
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05422402

反応ノート

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