Reaktion #432106
ord-eb544e38ca964e91b097a82135e1ebc8
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeA mixture was prepared
- 2SonstigeAfter an exothermic reaction
- 3workup.ADDITIONfollowed by dropwise addition of the solution which
- 4Sonstigewas prepared
- 5workup.ADDITIONThe addition
- 6workup.STIRRINGThe reaction mixture was stirred for 1 hour
- 7Temperaturby heating for further 1 hour
- 8workup.ADDITIONwas added
- 9workup.STIRRINGstirred overnight
- 10Extraktionextracted with diethylether
- 11WaschenThe extract was washed with an aqueous solution saturated with NaCl
- 12Trocknendried with sodium sulfate
- 13Einengenconcentrated
- 14workup.DISTILLATIONThe concentrate was distilled under reduced pressure
Vorschrift
A mixture was prepared by suspending 7.2 g of metallic magnesium into 40 ml of tetrahydrofuran (THF). The mixture, wherein 1 ml of 2-bromo-4-ethylanisole was added, was stirred at room temperature. After an exothermic reaction occurred, the reaction mixture was diluted with 100 ml of THF, followed by dropwise addition of the solution which was prepared by dissolving 63.5 g of 2-bromo-4-ethylanisole into 160 ml of THF. The addition was took 2 hours. The reaction mixture was stirred for 1 hour, reflexed by heating for further 1 hour and cooled down to 0° C. in internal temperature, wherein 59 g of p-bromoanisole was added thereinto, 0.5 g power of the complex compound of nickel chloride and 1,3-diphenylphosphynopropane (Nidppp Cl2) was added in the reaction mixture, and stirred overnight. The reactant was transferred into ammonium chloride water solution and extracted with diethylether. The extract was washed with an aqueous solution saturated with NaCl, dried with sodium sulfate and concentrated. The concentrate was distilled under reduced pressure to yield 51.6 g of 5-ethyl-2,4'-dimethoxy-biphenyl having a b.p. of 135°-148° C. (0.5 mmHg).