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Guaiacol → (2-Methoxyphenoxy)acetonitrile

HRID 1824308
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HRID 1824308 반응식
C(=O)([O-])[O-].[K+].[K+].[CH3:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[OH:15].Br[CH2:17][C:18]#[N:19]>CC(C)=O>[C:18]([CH2:17][O:15][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[O:8][CH3:7])#[N:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 460GuaiacolHCID 11430Potassium CarbonateHCID 11534Bromoacetonitrile

생성물 1

HCID 2736747(2-Methoxyphenoxy)acetonitrile수율 84.2%

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

Potassium carbonate (24 g) was added to a solution of of 2-methoxy phenol (18.94 g, 0.152 mol) in acetone (500 ml) at room temperature. A solution of bromoacetonitrile (17.43 g, 0.145 mol) in acetone (500 ml) was then added and the resulting suspension was heated at reflux for 10 h. The reaction vessel was then cooled and the solution was concentrated under reduced pressure and taken up into water (150 ml). Chloroform (250 ml) was added and the two layers separated. The organic phase was washed with brine (100 ml) and 10% aqueous NaOH (100 ml). The organic phase was dried (MgSO4) and concentrated under reduced pressure to give the product (19.91 g, 80%) as an oil. 1H NMR (CDCl3, 250 MHz) 7.0 (4H m), 4.8 (2H, s), 3.9 (3H, s).

후처리

  1. temperaturethe resulting suspension was heated
  2. temperatureat reflux for 10 h
  3. temperatureThe reaction vessel was then cooled
  4. concentrationthe solution was concentrated under reduced pressure
  5. additionChloroform (250 ml) was added
  6. customthe two layers separated
  7. washThe organic phase was washed with brine (100 ml) and 10% aqueous NaOH (100 ml)
  8. dry with materialThe organic phase was dried (MgSO4)
  9. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3df7fb7bb7b64d21a9d995366e78addf
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07041684B2

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