Reaktion #656546

ord-4f2a8dd08dc64f9ab7d7aee25555af48

Reaktionsgleichung

O
water
CC(=O)C(=NOCC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate
CCOCC.FB(F)F
boron trifluoride diethyl etherate
Br.c1cc[nH+]cc1
pyridinium hydrobromide
O=C(CON=C(C(=O)O)C(=O)CBr)OCc1ccccc1
2-benzyloxycarbonylmethoxyimino-4-bromo-3-oxobutyric acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted twice with ethyl acetate (70 ml)
  2. 2
    WaschenThe combined extracts were washed with 10% hydrochloric acid
  3. 3
    Trocknenby drying over magnesium sulfate
  4. 4
    SonstigeRemoval of the solvent

Vorschrift

To a solution of tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate (2.0 g) in dry tetrahydrofuran (20 ml) were added boron trifluoride diethyl etherate (3.0 ml) and pyridinium hydrobromide perbromide (3.0 g) at ambient temperature, followed by stirring for 6 hours. The reaction mixture was poured into water (50 ml) and then extracted twice with ethyl acetate (70 ml). The combined extracts were washed with 10% hydrochloric acid and then a saturated aqueous sodium chloride, followed by drying over magnesium sulfate. Removal of the solvent gave 2-benzyloxycarbonylmethoxyimino-4-bromo-3-oxobutyric acid (2.0 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04731443uspto-grants-1988_03