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5-Chloromethylfurfural → 5-Acetoxymethyl-2-furaldehyde

HRID 1051033
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1051033
Cl[CH2:2][C:3]1[O:9][C:6]([CH:7]=[O:8])=[CH:5][CH:4]=1.[C:10]([O-:13])(=[O:12])[CH3:11].C([N+]1C=CN(C)C=1)C>CC#N>[C:10]([O:13][CH2:2][C:3]1[O:9][C:6]([CH:7]=[O:8])=[CH:5][CH:4]=1)(=[O:12])[CH3:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 741915-Chloromethylfurfural2×HCID 178476379HCID 178476379, Verbindung

Produkt 1

HCID 663495-Acetoxymethyl-2-furaldehyde

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

In a round flask, 2 mL of methyl cyanide (acetonitrile) as an organic solvent was introduced, 0.145 g (1 mmol) of 5-chloromethylfurfural (CMF, compound I) was dissolved in the organic solvent, 0.170 g (1 mmol) of 1-ethyl-3-methylimidazolium acetate was added to the solution, and then the mixed solution was reacted at normal pressure and room temperature for 5 minutes. After the reaction, the reaction product was extracted by the addition of a small amount of water (5 mL) and ethyl acetate (added twice by 20 mL) to obtain an organic layer. The obtained organic layer was concentrated under reduced pressure to obtain light yellow liquid 5-acetoxymethylfurfural (AcHMF, compound II). The yield thereof is 36%.

Aufarbeitung

  1. additionwas added to the solution
  2. customthe mixed solution was reacted at normal pressure and room temperature for 5 minutes
  3. customAfter the reaction
  4. extractionthe reaction product was extracted by the addition of a small amount of water (5 mL) and ethyl acetate (
  5. additionadded twice by 20 mL)
  6. customto obtain an organic layer
  7. concentrationThe obtained organic layer was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-fa13fc02b128447c81c9ce0551e8f51c
Quelldatensatz
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09388150B2

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