Benzaldehyde → HCID 15224426, compound

HRID 2119872Notes

Reaction equation

HRID 2119872 reaction equation
[CH3:1][CH:2]([CH3:17])[CH2:3][N:4]1[C:16]2[C:15]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[N:9]=[CH:8][C:7]=2[N:6]=[CH:5]1.C([Li])CCC.[CH:23](=[O:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>O1CCCC1>[CH3:1][CH:2]([CH3:17])[CH2:3][N:4]1[C:16]2[C:15]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[N:9]=[CH:8][C:7]=2[N:6]=[C:5]1[CH:23]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[OH:30]

Participants

5

Reactant 3

HCID 240BenzaldehydeHCID 11424651DeaminoimiquimodHCID 178418339Butyllithium

Product 1

HCID 15224426HCID 15224426, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-78 °C

Procedure

1-(2-Methylpropyl)-1H-imidazo[4,5-c]quinoline (4 g; 0.017 mol) was dissolved in tetrahydrofuran (50 mL) then cooled to −78° C. A 7.75 mL portion of n-butyl lithium (2.5 M in hexanes) was added dropwise to the cooled solution. At 15 minutes post addition, benzaldehyde (2.7 mL; 0.027 mol) was added and the reaction mixture was allowed to warm slightly. The reaction was quenched with water then diluted with ethyl ether. The ether was separated, dried with magnesium sulfate then concentrated under vacuum. The resulting residue was purified by silica gel chromatography using 5% methanol in methylene chloride as the eluent to give an oily yellow solid. This material was recrystallized from methylene chloride/hexane to provide a white crystalline solid, m.p. 160-166° C. Analysis: Calculated: C, 76.1; H, 6.4; N, 12.7; Found: C, 75.9; H, 6.3; N, 12.7.

Workup

  1. additionwas added
  2. temperatureto warm slightly
  3. customThe reaction was quenched with water
  4. additionthen diluted with ethyl ether
  5. customThe ether was separated
  6. dry with materialdried with magnesium sulfate
  7. concentrationthen concentrated under vacuum
  8. customThe resulting residue was purified by silica gel chromatography
  9. customto give an oily yellow solid
  10. customThis material was recrystallized from methylene chloride/hexane
  11. customto provide a white crystalline solid, m.p. 160-166° C

Sources & evidence

ORD record
ord-f76039a322654c42a45daf469e48e839
Source dataset
uspto-grants-2004_02
Patent number
US06686472B2

Reaction notes

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