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Chloroacetonitrile → 3,4-Dimethoxyphenoxyacetonitrile

HRID 458792
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HRID 458792 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([OH:11])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].Cl[CH2:13][C:14]#[N:15].C([O-])([O-])=O.[K+].[K+].CCOC(C)=O.CCCCCC>CC(C)=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:6]=[CH:7][C:8]=1[O:9][CH3:10])[O:11][CH2:13][C:14]#[N:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7856ChloroacetonitrileHCID 11430Potassium CarbonateHCID 162513,4-DimethoxyphenolHCID 21226206Ethyl acetate hexane

생성물 1

HCID 189913533,4-Dimethoxyphenoxyacetonitrile수율 71.9%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a solution of 3,4-dimethoxyphenol (5.0 g, 32.4 mmol) in dry acetone (160 ml), were added chloroacetonitrile (2.05 ml, 32.4 mmol) and anhydrous K2CO3 (6.72 g, 48.6 mmol). The reaction mixture was stirred at reflux for 20 h under nitrogen. After cooling, the mixture was filtered and concentrated in vacuo. The residue was combined with H2O, extracted with CH2Cl2, and the combined organic phases were dried over anhydrous MgSO4, filtered and concentrated to give a crude oil. Flash chromatography (AcOEt/hexane: 3/7) gave the title product (4.5 g, 68%).

후처리

  1. temperatureat reflux for 20 h under nitrogen
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered
  4. concentrationconcentrated in vacuo
  5. extractionextracted with CH2Cl2
  6. dry with materialthe combined organic phases were dried over anhydrous MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customto give a crude oil

출처 및 근거

ORD 기록
ord-8816e7b744094312af3b119e1ef6e794
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07192950B2

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