Diethyl Ether → Dimethylcurcumin

HRID 1006708Notes

Reaction equation

HRID 1006708 reaction equation
[CH3:1][O:2][C:3]1C(O)=C[CH:6]=[C:5](/[CH:10]=[CH:11]/[C:12]([CH2:14][C:15](/[CH:17]=[CH:18]/[C:19]2[CH:27]=[C:24]([O:25][CH3:26])[C:22]([OH:23])=[CH:21][CH:20]=2)=[O:16])=[O:13])[CH:4]=1.[N+](=[CH2:30])=[N-].C[CH2:32][O:33][CH2:34][CH3:35]>CO>[CH3:32][O:33][C:34]1[CH:35]=[CH:6][C:5](/[CH:10]=[CH:11]/[C:12](/[OH:13])=[CH:14]/[C:15](/[CH:17]=[CH:18]/[C:19]2[CH:20]=[CH:21][C:22]([O:23][CH3:30])=[C:24]([O:25][CH3:26])[CH:27]=2)=[O:16])=[CH:4][C:3]=1[O:2][CH3:1]

Participants

5

Reactant 3

HCID 3283Diethyl Ether2×HCID 9550DiazomethaneHCID 969516Curcumin

Product 1

HCID 6477182DimethylcurcuminYield 19.8%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Curcumin (1) in Et2O and MeOH was treated with excess of diazomethane in ether for 24 h. The solvents were removed in vacuo and the residue was purified by silica gel column chromatography and PLC to yield yellow needles of 4 (yield 19.8%); mp 129-130° C. (MeOH) (Roughley et al., J. Chem. Soc. Perkin I, 2379-2388 (1973))(128-130° C.); 1H NMR (300 MHz, CDCl3): δ 3.93 (12H, s, OCH3×4), 5.82 (1H, s, 1-H), 6.48 (2H, d, 16 Hz), 6.88 (2H, d, J=8 Hz), 7.08 (2H, bs), 7.15 (2H, bd), 7.61 (2H, J=16 Hz); 13CNMR (300 MHz, CDCl3): δ 55.9, 56.0, 101.3, 109.8, 111.1, 122.0, 122.6, 128.1, 140.4, 149.2, 151.0, 183.2.

Workup

  1. customThe solvents were removed in vacuo
  2. customthe residue was purified by silica gel column chromatography and PLC

Sources & evidence

ORD record
ord-7653e02a991f4afc84ad2efaa2e0ca9b
Source dataset
uspto-grants-2004_09
Patent number
US06790979B2

Reaction notes

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