Piperonal → methyl(Z)-3-(3,4-methylenedioxyphenyl)-2-[3-(prop-1-yloxy)benzoyl]propenoate

HRID 862346Notes

Reaction equation

HRID 862346 reaction equation
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH:10]=[C:11]([C:16](=[O:27])[C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([O:23][CH2:24][CH2:25][CH3:26])[CH:18]=3)[C:12]([O:14][CH3:15])=[O:13])=[CH:4][C:3]=2[O:2]1.COC(=O)CC(=O)C1C=CC=C(OCCC)C=1.C1OC2C=CC(C=O)=CC=2O1>C1C=CC=CC=1.C(O)(=O)C.N1CCCCC1>[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5](/[CH:10]=[C:11](/[C:16](=[O:27])[C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([O:23][CH2:24][CH2:25][CH3:26])[CH:18]=3)\[C:12]([O:14][CH3:15])=[O:13])=[CH:4][C:3]=2[O:2]1

Participants

7

Procedure

Methyl 3-(3,4-methylenedioxyphenyl)-2-[3-(prop-1-yloxy)benzoyl]propenoate. To a solution of methyl-3-(Prop-1-yloxy)benzoylacetate (10 g, 4.2 mmol) in benzene (50 mL) was added 3,4-methylenedioxybenzaldehyde (6.36 g, 4.2 mmol) followed by piperidine (0.42 mL, 0.42 mmol) and glacial acetic acid (8 drops approx.). The mixture was refluxed for 2 h. and the volatiles removed in vacuo to give methyl (Z)-3-(3,4-methylenedioxyphenyl)-2-[3-(prop-1-yloxy)benzoyl]propenoate (7.4 g, 48%) as an off white solid after trituration with methanol (m.p. 122°-123° C.). Anal. Calc. for C21H20O6 : C, 68.47; H, 5.47. Found: C, 68.81; H, 5.49.

Workup

  1. temperatureThe mixture was refluxed for 2 h.
  2. customthe volatiles removed in vacuo

Sources & evidence

ORD record
ord-c3b2290ca7d4425a940a734a522d12c8
Source dataset
uspto-grants-1998_02
Patent number
US05716984

Reaction notes

Loading…