Iodoethane → HCID 57855844, compound

HRID 475574Notes

Reaction equation

HRID 475574 reaction equation
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10](=[O:27])[CH2:11][CH2:12][C:13]1[N:14]=[C:15]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[C:20]([OH:26])[CH:19]=2)[O:16][CH:17]=1)[CH3:2].N12CCCN=C1CCC[CH2:30][CH2:29]2.C(I)C>C(O)C>[CH2:29]([O:26][C:20]1[CH:19]=[C:18]([C:15]2[O:16][CH:17]=[C:13]([CH2:12][CH2:11][C:10]([C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=3[O:3][CH2:1][CH3:2])=[O:27])[N:14]=2)[CH:23]=[CH:22][C:21]=1[O:24][CH3:25])[CH3:30]

Participants

5

Procedure

A 0.3 g quantity of 1-(2-ethoxyphenyl)-3-[2-(3-hydroxy-4-methoxyphenyl)oxazol-4-yl]propan-1-one obtained in Example 101 was suspended in 10 ml of ethanol, 0.37 g of 1,8-diazabicyclo[5,4,0]undec-7-ene and 0.26 g of ethyl iodide were added thereto, and the suspension was stirred for 4 hours while heating and refluxing. After distilling off ethanol under reduced pressure, water was added, ethyl acetate extraction was performed, followed by drying over anhydrous magnesium sulfate and distilling the solvent off. The residue was subjected to silica gel column purification (n-hexane:ethyl acetate=3:1), thereby yielding 0.15 g of white powdery 3-[2-(3-ethoxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-ethoxyphenyl)propan-1-one.

Workup

  1. temperaturewhile heating
  2. temperaturerefluxing
  3. distillationAfter distilling off ethanol under reduced pressure, water
  4. additionwas added
  5. extractionethyl acetate extraction
  6. dry with materialby drying over anhydrous magnesium sulfate
  7. distillationdistilling the solvent off
  8. customThe residue was subjected to silica gel column purification (n-hexane:ethyl acetate=3:1)

Sources & evidence

ORD record
ord-cc1019f7ce154cd6a49aa62b6897f8f5
Source dataset
uspto-grants-2014_01
Patent number
US08637559B2

Reaction notes

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