Reaktion #2358454

ord-f59dd24e8e8b469b9585b26249e1029a

Reaktionsgleichung

CCOC(=O)CC(=O)c1c(F)cc(F)c(F)c1C
ethyl 2-methyl-3,4,6-trifluorobenzoylacetate
CC(=O)OC(C)=O
acetic anhydride
CCOC([O-])[O-]
ethyl orthoformate
CCOC=C(C(=O)OCC)C(=O)c1c(F)cc(F)c(F)c1C
ethyl 2-(2-methyl-3,4,6-trifluorobenzoyl)-3-ethoxyacrylate
Ausbeute 90.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturby heating
  2. 2
    Temperaturrefluxing for 1 hour
  3. 3
    EinengenThe resulting mixture was concentrated

Vorschrift

To 3.2 g of ethyl 2-methyl-3,4,6-trifluorobenzoylacetate were added 3.0 g of acetic anhydride and 2.7 g of ethyl orthoformate, followed by heating and refluxing for 1 hour. The resulting mixture was concentrated to give 3.5 g of ethyl 2-(2-methyl-3,4,6-trifluorobenzoyl)-3-ethoxyacrylate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06333431B1uspto-grants-2001_12