Hydrochloric Acid → 2,3-Dicyano-4-octyloxyphenol

HRID 1755623노트

반응식

HRID 1755623 반응식
[Na].[C:2]([C:4]1[C:10]([C:11]#[N:12])=[C:9]([OH:13])[CH:8]=[CH:7][C:5]=1[OH:6])#[N:3].[O-]CC.[I-].[K+].[CH2:19](Br)[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26].Cl>C(O)C.O>[C:2]([C:4]1[C:10]([C:11]#[N:12])=[C:9]([O:13][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH:8]=[CH:7][C:5]=1[OH:6])#[N:3]

참가 물질

9

실험 절차

Sodium (1.15 g, 50 mmoles) was reacted with anhydrous ethanol (200 mL) under a nitrogen atmosphere. 2,3-dicyanohydroquinone (8.01 g, 50 mmoles) in anhydrous ethanol (50 mL) was added dropwise to the ethoxide solution. Upon completion of the addition, potassium iodide (0.5 g) in 5 mL water was added. This solution was brought to reflux and octyl bromide (9.66 g, 50 mmoles) was added dropwise. The reaction was then refluxed under nitrogen atmosphere for one day. The mixture was acidified with 0.5N aqueous HCl and the solvents were removed under reduced pressure. The crude reaction mixture was flash chromatographed using silica gel and methylene chloride as eluent. The appropriate fractions containing the desired product, 2,3-dicyano-4-octyloxyphenol, were combined and the solvent removed under reduced pressure on a rotary evaporator. The crude product was recrystallized from ethanol/water to give 4.5 g 2,3-dicyano-4-octyloxyphenol.

후처리

  1. additionwas added
  2. temperatureto reflux
  3. temperatureThe reaction was then refluxed under nitrogen atmosphere for one day
  4. customthe solvents were removed under reduced pressure
  5. customThe crude reaction mixture
  6. customchromatographed
  7. additionThe appropriate fractions containing the desired product, 2,3-dicyano-4-octyloxyphenol
  8. customthe solvent removed under reduced pressure on a rotary evaporator
  9. customThe crude product was recrystallized from ethanol/water

출처 및 근거

ORD 기록
ord-c8a89128055f49f18df994f156aec327
출처 데이터셋
uspto-grants-1995_08
특허 번호
US05437812

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