Toluene → 3-Cyclohexylpropyl 3-(1H-imidazol-4-yl)propyl ether

HRID 726227

반응식

HRID 726227 반응식
C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:8]2[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15][O-:16])[N:10]=[CH:9]2)C=CC=CC=1.[Na+].C1(C)C=CC=CC=1.C1OCCOCCOCCOCCOC1.Cl[CH2:53][CH2:54][CH2:55][CH:56]1[CH2:61][CH2:60][CH2:59][CH2:58][CH2:57]1>C(OCC)C>[NH:8]1[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15][O:16][CH2:53][CH2:54][CH2:55][CH:56]2[CH2:61][CH2:60][CH2:59][CH2:58][CH2:57]2)[N:10]=[CH:9]1

참가 물질

6

반응 조건

온도
75 °C

실험 절차

5 mmol of sodium 3-[1-(triphenylmethyl)imidazol-4-yl]propoxide in 10 ml of toluene containing 0.5 mmol of 15-Crown-5 and 5 mmol of (3-chloropropyl)cyclohexane are mixed and the mixture is stirred for 24 h at 75° C. The suspension is concentrated under vacuum, the product obtained is dissolved in diethyl ether, the solution is filtered and the residue washed with petroleum ether (40°-60° C.). The filtrate obtained is concentrated and maintained for 1 h at the boiling point in a 2N aqueous/alcohol (ethanol/water) hydrochloric acid solution. The ethanol is removed under a low vacuum and the precipitate is filtered under vacuum. The solution is basified, extracted with dichloromethane and the organic phase is concentrated. The title compound obtained is recrystallized in the hydrogenmaleate form from ethanol/ diethyl ether.

후처리

  1. concentrationThe suspension is concentrated under vacuum
  2. customthe product obtained
  3. filtrationthe solution is filtered
  4. washthe residue washed with petroleum ether (40°-60° C.)
  5. customThe filtrate obtained
  6. concentrationis concentrated
  7. temperaturemaintained for 1 h at the boiling point in a 2N aqueous/alcohol (ethanol/water) hydrochloric acid solution
  8. customThe ethanol is removed under a low vacuum
  9. filtrationthe precipitate is filtered under vacuum
  10. extractionextracted with dichloromethane
  11. concentrationthe organic phase is concentrated

출처 및 근거

ORD 기록
ord-f5a0acaa7b8148ff8e717fa1d8a06de0
출처 데이터셋
uspto-grants-1998_01
특허 번호
US05708171

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