Ethylene Glycol → HCID 59665583, Verbindung

HRID 1011350Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1011350
[O:1]=[C:2]1[C:10]2[C:5](=[N:6][C:7]([CH:11]=[O:12])=[CH:8][CH:9]=2)[CH2:4][O:3]1.[CH2:13](O)[CH2:14][OH:15].O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C([O-])(O)=O.[Na+]>C1C=CC=CC=1>[O:12]1[CH2:13][CH2:14][O:15][CH:11]1[C:7]1[N:6]=[C:5]2[CH2:4][O:3][C:2](=[O:1])[C:10]2=[CH:9][CH:8]=1

Komponenten

6

Edukt 4

HCID 174Ethylene GlycolHCID 516892Sodium BicarbonateHCID 521998p-Toluenesulfonic acid monohydrateHCID 58478784HCID 58478784, Verbindung

Produkt 1

HCID 59665583HCID 59665583, VerbindungAusbeute 33,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

To a solution of 5-oxo-5,7-dihydro-furo[3,4-b]pyridine-2-carbaldehyde (100 mg, 0.61 mmol) in anhydrous benzene (5 mL) is added ethylene glycol (0.1 mL, 1.77 mmol), a catalytic amount p-toluenesulfonic acid monohydrate and 4 Å mole sieves. The reaction mixture is heated at a reflux temperature for 20 h. The reaction mixture is allowed to cool to room temperature and saturated aqueous NaHCO3 solution is added. The resulting mixture is filtered through celite, washed with saturated aqueous NaHCO3 and EtOAc. The isolated organic layer is washed with brine (1×), dried with anhydrous Na2SO4, and concentrated. The residue is treated with EtOAc-Hexane (1:4) and the light brown solid which forms is collected by filtration and dried to give the title compound (42 mg, 33%).

Aufarbeitung

  1. temperatureThe reaction mixture is heated at a reflux temperature for 20 h
  2. filtrationThe resulting mixture is filtered through celite
  3. washwashed with saturated aqueous NaHCO3 and EtOAc
  4. washThe isolated organic layer is washed with brine (1×)
  5. dry with materialdried with anhydrous Na2SO4
  6. concentrationconcentrated
  7. additionThe residue is treated with EtOAc-Hexane (1:4)
  8. filtrationthe light brown solid which forms is collected by filtration
  9. customdried

Quellen und Nachweise

ORD-Eintrag
ord-4d7993839afa4c50839dc5986be2c9cb
Quelldatensatz
uspto-grants-2011_07
Patentnummer
US07977351B2

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