Reaction equation
C(C1C(=O)C(Cl)=C(Cl)C(=O)C=1C#N)#N.[OH:15][C:16]1[C:24]([CH:25]=[O:26])=[CH:23][C:19]2[CH2:20][CH2:21][O:22][C:18]=2[C:17]=1[O:27][CH3:28]>O1CCOCC1>[OH:15][C:16]1[C:24]([CH:25]=[O:26])=[CH:23][C:19]2[CH:20]=[CH:21][O:22][C:18]=2[C:17]=1[O:27][CH3:28]Participants
Procedure
A solution of 817 mg. (3.6 mmole) of DDQ in 10 ml. of dioxane was added to 582 mg. (3 mmole) of 2,3-dihydro-6-hydroxy-7-methoxy-5-benzofuran-carboxaldehyde in 15 ml. of dioxane and the resulting mixture was heated under reflux for 7 hours, cooled and the formed solid removed by filtration. The precipitate was thoroughly washed first with benzene, then with CHCl3. The washings were combined with the initial filtrate and the total concentrated in vacuo to a residue which was chromatographed first on a 20 ml. dry silica gel column (E. Merck 7734) with CHCl3 elution followed by conventional chromatography over 20 g. of silica (E. Merck 7734) packed in benzene-ethyl acetate (95:5) and elution with this solvent mixture provided, after workup, a yellow solid, m.p. 60°-62°.
Workup
- temperatureunder reflux for 7 hours
- temperaturecooled
- customthe formed solid removed by filtration
- washThe precipitate was thoroughly washed first with benzene
- concentrationthe total concentrated in vacuo to a residue which
- customwas chromatographed first on a 20 ml
- washdry silica gel column (E. Merck 7734) with CHCl3 elution
- washelution with this solvent mixture
- customprovided
Sources & evidence
- ORD record
- ord-faaced70dcaa4b2b8d73c3c300f64d98
- Source dataset
- uspto-grants-1979_04
- Patent number
- US04150042
Linked notes
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