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Ethylene Glycol → HCID 3525985, 화합물

HRID 1521745
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HRID 1521745 반응식
[O:1]=[C:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[CH2:3][C:4]#[N:5].[CH2:12](O)[CH2:13][OH:14]>C1(C)C=CC=CC=1.CC1C=CC(S(O)(=O)=O)=CC=1>[C:6]1([C:2]2([CH2:3][C:4]#[N:5])[O:14][CH2:13][CH2:12][O:1]2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 174Ethylene GlycolHCID 64799Benzoylacetonitrile

생성물 1

HCID 3525985HCID 3525985, 화합물수율 77%

시약·촉매·용매 2

HCID 6101p-Toluenesulfonic acid촉매HCID 1140Toluene용매

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온도
150 °C

실험 절차

To a solution of 3-oxo-3-phenylpropanenitrile (10 g, 69 mmol) and PTSA (27 mg, 1.37 mmol) in toluene (120 mL) is added ethylene glycol (120 mL, 2057 mmol). The azeotropic mixture is heated at 150° C. for 14 h. The solvent is evaporated under reduced pressure and the residue is washed with 10% aqueous NaOH solution. The aqueous layer is extracted with diethyl ether (2×100 mL) and the combined organic layers are dried (Na2SO4) and evaporated to provide the crude compound. The crude material is purified over neutral alumina eluting with 1% of ethyl acetate/hexane to afford the title compound as an off-white solid (10 g, 77%).

후처리

  1. customThe solvent is evaporated under reduced pressure
  2. washthe residue is washed with 10% aqueous NaOH solution
  3. extractionThe aqueous layer is extracted with diethyl ether (2×100 mL)
  4. dry with materialthe combined organic layers are dried (Na2SO4)
  5. customevaporated
  6. customto provide the crude compound
  7. customThe crude material is purified over neutral alumina eluting with 1% of ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-2121c895708f495f932c6351e5b1841d
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073926B2

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