Reaktion #1675332

Reaktionsgleichung

ethyl acetate n-hexane

tetrahydrofuran isopropanol

hydrogen chloride

1,4-dimethoxy-2,5-bis(methoxymethoxy)-3-methyl-6-{5-[2,5-dimethoxy-3,6-bis(methoxymethoxy)phenyl]pentyl}benzene

→

2,5-dimethoxy3-methyl-6-[5-(2,5-dimethoxy-1,4-benzoquinon-3-yl)pentyl]1,4-benzoquinone

Lösungsmittel

isopropanol

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe solvent was removed by evaporation under reduced pressure
2. 2
   Sonstigeto obtain colorless powdery substance
3. 3
   workup.DISSOLUTIONThis substance was dissolved
4. 4
   Sonstigewithout being purified, in 20 ml of methanol
5. 5
   workup.ADDITIONa small amount of sodium hydrogen carbonate was added
6. 6
   Temperaturthe mixture was heated at 60° C.
7. 7
   workup.STIRRINGwas stirred for 2 hours under oxygen gas stream condition
8. 8
   SonstigeThe solvent was removed by evaporation under reduced pressure
9. 9
   Sonstigethe residue obtained

Vorschrift

426 Milligrams of 1,4-dimethoxy-2,5-bis(methoxymethoxy)-3-methyl-6-{5-[2,5-dimethoxy-3,6-bis(methoxymethoxy)phenyl]pentyl}benzene was dissolved in 5 ml of tetrahydrofuran and 5 ml of isopropanol, under nitrogen gas stream conditions, 1 ml of tetrahydrofuran-isopropanol (1:1) solution of 20% hydrogen chloride was added thereto, and the mixture was stirred at room temperature for 12 hours. The solvent was removed by evaporation under reduced pressure to obtain colorless powdery substance. This substance was dissolved, without being purified, in 20 ml of methanol, and a small amount of sodium hydrogen carbonate was added, then the mixture was heated at 60° C., and was stirred for 2 hours under oxygen gas stream condition. The solvent was removed by evaporation under reduced pressure, and the residue obtained was developed on a preparative thin layer chromatography (eluent: 40% ethyl acetate-n-hexane) to obtain 262 mg of 2,5-dimethoxy3-methyl-6-[5-(2,5-dimethoxy-1,4-benzoquinon-3-yl)pentyl]1,4-benzoquinone. Yellow powdery substance.

Quelle