Kojic Acid → 5-(4-Chloro-benzyloxy)-2-hydroxymethyl-pyran-4-one

HRID 250649

Reaktionsgleichung

Reaktionsgleichung von HRID 250649
[CH:1]1[C:6](=[O:7])[C:5]([OH:8])=[CH:4][O:3][C:2]=1[CH2:9][OH:10].[Cl:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16]Br)=[CH:14][CH:13]=1.[OH-].[Na+]>CO.O>[Cl:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16][O:8][C:5]2[C:6](=[O:7])[CH:1]=[C:2]([CH2:9][OH:10])[O:3][CH:4]=2)=[CH:14][CH:13]=1

Komponenten

6

Edukt 3

HCID 3840Kojic AcidHCID 14798Sodium HydroxideHCID 693291-(Bromomethyl)-4-chlorobenzene

Produkt 1

HCID 580868345-(4-Chloro-benzyloxy)-2-hydroxymethyl-pyran-4-one

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Kojic acid (637, 5.00 g, 35.2 mmol) and 4-chlorobenzyl bromide (557, 7.95 g, 38.7 mmol) were suspended in methanol (40 mL) in an 80 mL sealed tube. Sodium hydroxide in water (12 M, 2.93 mL) was added. The reaction was heated at 80° C. overnight. The resulting suspension was concentrated. Water was added and the mixture was filtered and washed with water to provide a brown solid. Washing with minimal methanol on the filter removed the brown color. A white solid (638, 7.58 g, 80%) was isolated. 1H-NMR was consistent with the desired compound.

Aufarbeitung

  1. customsealed tube
  2. concentrationThe resulting suspension was concentrated
  3. additionWater was added
  4. filtrationthe mixture was filtered
  5. washwashed with water
  6. customto provide a brown solid
  7. washWashing with minimal methanol on the filter
  8. customremoved the brown color
  9. customA white solid (638, 7.58 g, 80%) was isolated

Quellen und Nachweise

ORD-Eintrag
ord-ba78ef01d4f24351b97ef40f64e88199
Quelldatensatz
uspto-grants-2011_01
Patentnummer
US07863288B2

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