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Acetic Anhydride → HCID 15007064, compound

HRID 1612655
Notes
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Reaction equation

HRID 1612655 reaction equation
[CH3:1][C:2]1[CH:11]([CH3:12])[C:10](=[O:13])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[C:14](OC(=O)C)(=[O:16])[CH3:15]>>[C:14]([O:13][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]([CH3:1])[C:11]=1[CH3:12])(=[O:16])[CH3:15]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 7918Acetic AnhydrideHCID 67692496HCID 67692496, compound

Product 1

HCID 15007064HCID 15007064, compound

Procedure

A solution of 1.73 g of 2,3-dimethyl-4-quinolone in 25 ml of acetic anhydride was stirred at 130° C. for 8 hours. The solution was evaporated to remove the solvent under reduced pressure, and 30 ml of chloroform was added to the solution. The mixture was washed with an aqueous saturated sodium hydrogen carbonate solution and water and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the crude product thus obtained was purified by silica gel column chromatography (Wako Gel C-200) to give 1.87 g of 4-acetoxy-2,3-dimethylquinoline.

Workup

  1. customThe solution was evaporated
  2. customto remove the solvent under reduced pressure, and 30 ml of chloroform
  3. additionwas added to the solution
  4. wash
The mixture was washed with an aqueous saturated sodium hydrogen carbonate solution and water
  • dry with materialdried over sodium sulfate
  • customThe solvent was evaporated under reduced pressure
  • customthe crude product thus obtained
  • customwas purified by silica gel column chromatography (Wako Gel C-200)
  • Sources & evidence

    ORD record
    ord-51f6a0981d584821b05ed2840834126c
    Source dataset
    uspto-grants-1993_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05190952

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes