Acetic Acid → HCID 23291362, compound

HRID 1602895Notes

Reaction equation

HRID 1602895 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-bd70ea3cdb01472c852b2f1f46605112
Source dataset
uspto-grants-1999_11
Patent number
US05985886

Reaction notes

Loading…