Potassium Carbonate → (5-Phenyl-benzoxazol-2-yl)methanol

HRID 1827990Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1827990
[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[O:14][C:13]([CH2:15][O:16]C(=O)C)=[N:12][C:11]=3[CH:20]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([O-])([O-])=O.[K+].[K+]>CO>[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[O:14][C:13]([CH2:15][OH:16])=[N:12][C:11]=3[CH:20]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Komponenten

4

Edukt 2

HCID 11430Potassium CarbonateHCID 20622383Acetic Acid 5-phenyl-benzoxazol-2-ylmethyl Ester

Produkt 1

HCID 22062842(5-Phenyl-benzoxazol-2-yl)methanolAusbeute 72,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

Acetic acid (5-phenyl-benzoxazol-2-yl)methyl ester 50 (409 mg, 1.53 mmol) was dissolved in 10 ml of methanol. Finely ground K2CO3 (53 mg, 0.38 mmol) was added. After 3 hrs, the mixture was concentrated then diluted with water and extracted with ethyl acetate. The extracts were washed with brine, dried, filtered and concentrated to yield about 251 mg of (5-phenyl-benzoxazole-2-yl)methanol 51.

Aufarbeitung

  1. concentrationthe mixture was concentrated
  2. additionthen diluted with water
  3. extractionextracted with ethyl acetate
  4. washThe extracts were washed with brine
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-b568d62fd2124687a428fd93d365a9fb
Quelldatensatz
uspto-grants-2006_06
Patentnummer
US07056903B2

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