Acetic Acid → 4-Acetyl-2-methoxyphenyl acetate

HRID 1891438Notes

Reaction equation

HRID 1891438 reaction equation
[CH3:1][C:2]([C:4]1[CH:12]=[CH:11][C:9]([OH:10])=[C:6]([O:7][CH3:8])[CH:5]=1)=[O:3].N1C=CC=CC=1.[C:19](O)(=[O:21])[CH3:20]>C1COCC1>[C:19]([O:10][C:9]1[CH:11]=[CH:12][C:4]([C:2](=[O:3])[CH3:1])=[CH:5][C:6]=1[O:7][CH3:8])(=[O:21])[CH3:20]

Participants

5

Reactant 3

HCID 176Acetic AcidHCID 1049PyridineHCID 2214Acetovanillone

Product 1

HCID 5215354-Acetyl-2-methoxyphenyl acetate

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

As shown in the above-described reaction formula, acetovanillone (500 mg, 3 mM) dissolved in 20 ml of THF was mixed with 0.5 ml of pyridine and 0.6 ml of anhydrous acetic acid. The mixture was stirred for 3 hours at room temperature. The resulting product was recovered with the extraction with diethylether and dried with anhydrous magnesium sulfate to remove remaining solvent. The remaining residue was performed to Silica gel column chromatography with a mobile phase (n-hexane:ethylacetate=4:1) to obtain white solid type of 4-acetyl-2-methoxyphenyl acetate (1; 625 mg).

Workup

  1. customThe resulting product was recovered with the extraction with diethylether
  2. dry with materialdried with anhydrous magnesium sulfate
  3. customto remove

Sources & evidence

ORD record
ord-27bfb0db101a44eea7969fd31c646267
Source dataset
uspto-grants-2013_08
Patent number
US08507553B2

Reaction notes

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