Reaktion #1667716

ord-e3dff9889de94634aa609c83bdfd0cee

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

40 grams (0.1 mol) of N-{α-(2,4-di-tert-amylphenoxy)acetyl} -m-aminoacetophenone (m.p.:135°C), obtained by the reaction between m-aminoacetophenone and α-(2,4-di-tert-amylphenoxy)acetyl chloride in pyridine, was dissolved in 200 ml of anhydrous ethyl ether (placed in a three-necked flask), and 0.5 g of anhydrous aluminum chloride powder was added to this solution followed by ice-cooling (about 0°-5°C) under stirring. 16 grams (0.1 mol) of bromine was added dropwise to this mixture. After the completion of the dropwise addition, the temperature was allowed to rise to room temperature (about 20°-35°C). Stirring was continued until the generation of hydrogen bromide stopped. Thus, white crystals were precipitated.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US03933500uspto-grants-1976_01