Cesium acetate → Acetic Acid 2-phenylbenzoxazol-5-ylmethyl Ester

HRID 1827995

Reaktionsgleichung

Reaktionsgleichung von HRID 1827995
Br[CH2:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[N:8][C:7]=2[CH:17]=1.[C:18]([O-:21])(=[O:20])[CH3:19].[Cs+]>CN(C=O)C>[C:11]1([C:9]2[O:10][C:6]3[CH:5]=[CH:4][C:3]([CH2:2][O:21][C:18](=[O:20])[CH3:19])=[CH:17][C:7]=3[N:8]=2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Komponenten

4

Edukt 2

HCID 5152919Cesium acetateHCID 220628305-Bromomethyl-2-phenylbenzoxazole

Produkt 1

HCID 23581212Acetic Acid 2-phenylbenzoxazol-5-ylmethyl EsterAusbeute 101,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

5-Bromomethyl-2-phenylbenzoxazole 56 (1.0 g, 3.4 mmol) and cesium acetate (1.33 g, 6.94 mmol) were stirred together in DMF(25 ml) under an atmosphere of N2 overnight. The DMF was evaporated under high vacuum and the residue partitioned between ethyl acetate (100 ml) and water (100 ml). The ethyl acetate layer was separated then washed and dried. Evaporation of the solvent yielded 920 mg of acetic acid 2-phenylbenzoxazol-5-ylmethyl ester 57.

Aufarbeitung

  1. customThe DMF was evaporated under high vacuum
  2. customthe residue partitioned between ethyl acetate (100 ml) and water (100 ml)
  3. customThe ethyl acetate layer was separated
  4. washthen washed
  5. customdried
  6. customEvaporation of the solvent

Quellen und Nachweise

ORD-Eintrag
ord-1a682e86b6b9402ca52d00ac51334d4e
Quelldatensatz
uspto-grants-2006_06
Patentnummer
US07056903B2

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