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

HRID 1058612
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HRID 1058612 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 174Ethylene GlycolHCID 516892Sodium BicarbonateHCID 27609212-(4-oxopiperidin-1-yl)acetonitrile

생성물 1

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

시약·촉매·용매 2

HCID 6101p-Toluenesulfonic acid촉매HCID 1140Toluene
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-1ae1f07031dc48a099b75ac4d4f0c37c
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06518265B1

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