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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1597736Erstellt: 25. Oktober 2026

Iodine → 1,1-Di(p-tolyl)ethylene

https://huagongshe.com/reaction/1597736

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktSulfuric AcidHCID 1118—
EduktIodoethaneHCID 6340—
Edukt4-BromotolueneHCID 7805—
Eduktp-METHYLACETOPHENONEHCID 8500—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1,1-Di(p-tolyl)ethyleneHCID 137765—

Reaktionsschritte

15.6 g (0.65 mol) of magnesium and 20 ml of THF were placed in a 1-liter reaction flask in a stream of nitrogen, the reaction was initiated with a small amount of ethyl iodide and iodine, and a solution of 111.15 g (0.65 mol) of p-bromotoluene in 500 ml of THF was added dropwise at a temperature from room temperature to 40° C. for 2 hours to prepare a Grignard reagent. A solution of 83.75 g (0.625 mol) of p-methylacetophenone (11c) in 200 ml of THF was added dropwise thereto at the same temperature for 3 hours. The resulting solution was stirred at room temperature for 3 hours, and subsequently stirred under reflux for 4 hours. Then, the solution was cooled, and poured into 1 liter of 5% aqueous sulfuric acid to conduct hydrolysis. The resulting product was extracted with toluene, and the extract was washed with aqueous soda ash, washed with water, and concentrated. Then, 300 ml of toluene and 0.5 g of PTSA were added thereto, followed by stirring under reflux for 4 hours to carry out azeotropic dehydration. The resulting product was washed with aqueous soda ash, washed with water, and concentrated. Crude 1,1-di(p-tolyl)ethylene (9c) was distilled in a Claisen flask equipped with a vigreux to obtain 98.5 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05736284
Quelldatensatzuspto-grants-1998_04
ORD IDord-f3012dea11b54feba994cbfa04ab3b5d
Quellennotizuspto-grants-1998_04