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Ethylene Glycol → 1,4-Dioxa-8-azaspiro[4.5]decane-8-acetonitrile

HRID 1058612
ノート
印刷プレビュー

反応式

HRID 1058612 の反応式
[O:1]=[C:2]1[CH2:7][CH2:6][N:5]([CH2:8][C:9]#[N:10])[CH2:4][CH2:3]1.[CH2:11](O)[CH2:12][OH:13].C(=O)([O-])O.[Na+]>C1(C)C=CC=CC=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>[CH2:11]1[CH2:12][O:13][C:2]2([CH2:7][CH2:6][N:5]([CH2:8][C:9]#[N:10])[CH2:4][CH2:3]2)[O:1]1
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 516892Sodium BicarbonateHCID 27609212-(4-oxopiperidin-1-yl)acetonitrile

生成物 1

HCID 186688031,4-Dioxa-8-azaspiro[4.5]decane-8-acetonitrile収率 97.1%

試薬・触媒・溶媒 2

HCID 6101p-Toluenesulfonic acid触媒HCID 1140Toluene
溶媒

実験手順

A solution of 10.0 g of 4-oxo-1-piperidineacetonitrile, 22.6 g of ethylene glycol and 0.62 g of anhydrous p-toluenesulfonic acid in 100 ml of toluene was refluxed for 6 hours with Dean-stark dehydrating apparatus. After cooling, the reaction mixture was added with saturated aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate. The extract was dried, and the solvent was evaporated to give a pale brown liquid. The resulting liquid was purified by alumina column chromatography using ethyl acetate—n-heptane (1:3) as an eluting solvent to give 12.8 g of a colorless liquid.

後処理

  1. temperatureAfter cooling
  2. extractionextracted with ethyl acetate
  3. customThe extract was dried
  4. customthe solvent was evaporated
  5. customto give a pale brown liquid
  6. customThe resulting liquid was purified by alumina column chromatography

出典と根拠

ORDレコード
ord-1ae1f07031dc48a099b75ac4d4f0c37c
出典データセット
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06518265B1

反応ノート

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