Ethyl ketone → 4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolane

HRID 31685

Reaktionsgleichung

Reaktionsgleichung von HRID 31685
[CH:1]1[CH:6]=[CH:5][C:4]([CH2:7][O:8][CH2:9][CH:10]([OH:13])[CH2:11][OH:12])=[CH:3][CH:2]=1.[CH3:14][CH2:15][C:16](=O)[CH2:17][CH3:18].O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)([O-])O.[Na+]>O1CCCC1>[CH2:7]([O:8][CH2:9][CH:10]1[CH2:11][O:12][C:16]([CH2:17][CH3:18])([CH2:15][CH3:14])[O:13]1)[C:4]1[CH:3]=[CH:2][CH:1]=[CH:6][CH:5]=1

Komponenten

6

Edukt 4

HCID 7288Ethyl ketoneHCID 980723-(Benzyloxy)-1,2-propanediolHCID 516892Sodium BicarbonateHCID 521998p-Toluenesulfonic acid monohydrate

Produkt 1

HCID 597925274-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolaneAusbeute 67,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a tetrahydrofuran (30 ml) solution of DL-α-O-benzyl glycerol (3 g, 16.5 mmol), 3-pentanone (17.5 ml, 165 mmol) and p-toluenesulfonic acid monohydrate (300 mg, 1.58 mmol) were added at room temperature and the mixture was stirred at the same temperature for 22 hours. To the reaction mixture, a saturated aqueous sodium hydrogen carbonate solution (5 ml) was added to adjust pH to about 8. The generated precipitate was removed by filtration and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (NH silica gel, elution solvent: heptane/ethyl acetate=1/0 to 3/1 gradient). A desired fraction was concentrated to obtain the title compound (2.77 g, 67.1% yield) as a colorless oil.

Aufarbeitung

  1. customThe generated precipitate was removed by filtration
  2. concentrationthe filtrate was concentrated
  3. customThe obtained residue was purified by silica gel column chromatography (NH silica gel, elution solvent: heptane/ethyl acetate=1/0 to 3/1 gradient)
  4. concentrationA desired fraction was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-b0ba235f52084fb9baa50225f74f6979
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07425634B2

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