Acetic Acid → HCID 23291362, compound

HRID 1586027Notes

Reaction equation

HRID 1586027 reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[C:9]2[O:11][CH2:12][O:13][C:8]2=[CH:7][C:4]=1[CH:5]=O.[C:14]([O:22][CH2:23][CH3:24])(=[O:21])[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17].N1CCCCC1.C(O)(=O)C>C1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:10]=[C:9]2[O:11][CH2:12][O:13][C:8]2=[CH:7][C:4]=1[CH:5]=[C:15]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[C:14]([O:22][CH2:23][CH3:24])=[O:21]

Participants

6

Procedure

A solution of the 2-methoxy-4,5-methylenedioxy benzaldehyde (16.0 g, 0.089 mol), diethyl malonate (15.0 ml, 0.090 mol), piperidine (4.4 ml, 0.044 mol) and acetic acid (2.5 ml, 0.045 mol) in benzene (75 ml) was stirred at reflux, equipped with a Dean-Stark apparatus, for 24 h. Upon removal of the solvent the crude residue was extracted with ethyl acetate and washed with 10% sodium carbonate solution, water, dried (Na2SO4). After removing the solvent, flash chromatography of the residue (silica gel, 25% ethyl acetate/hexane) provided the title compound as a yellow solid (26.0 g, 91%).

Workup

  1. temperatureat reflux
  2. customequipped with a Dean-Stark apparatus, for 24 h
  3. customUpon removal of the solvent the crude residue
  4. extractionwas extracted with ethyl acetate
  5. washwashed with 10% sodium carbonate solution, water
  6. dry with materialdried (Na2SO4)
  7. customAfter removing the solvent, flash chromatography of the residue (silica gel, 25% ethyl acetate/hexane)

Sources & evidence

ORD record
ord-07e28c3f62e949e1a2971fa62ae7ac26
Source dataset
uspto-grants-1999_08
Patent number
US05942516

Reaction notes

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