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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 746197Erstellt: 25. Oktober 2026

Methyl iodide → P-tert-Butoxy-alpha-methyl styrene

https://huagongshe.com/reaction/746197

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukttert-Butyl peroxybenzoateHCID 11966—
Edukt4-Chloro-alpha-methylstyreneHCID 74381—
EduktMagnesiumHCID 5462224—
Edukt4,4'-DiisopropenylbiphenylHCID 13422373—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktP-tert-Butoxy-alpha-methyl styreneHCID 1120629169,3%

Reaktionsschritte

The procedure of Example 1 was repeated, except that there was utilized 16.9 grams (0.70 mole) of magnesium metal and 100 grams (0.66 mole) of 4-chloro-α-methylstyrene dissolved in 200 ml. of tetrahydrofuran. The Grignard reaction was started by the addition of a small amount of methyl iodide. After the reaction mixture had been refluxed for 12 hours, there was added at 0° C. in a dropwise manner a solution of 85 grams of t-butylperbenzoate in 300 ml. of ethylether. A crystalline product identified as 4,4'-diisopropenylbiphenyl was isolated from the oil which was recovered by filtering the mixture and washing with methanol. After stripping the methanol, a 69.3% yield of 4-t-butoxy-α-methylstyrene was isolated by fractional distillation as a colorless liquid having a boiling point of 65°-68° C. at 0.03 millimeters.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04603101
Quelldatensatzuspto-grants-1986_07
ORD IDord-63997216ebee447ba405a25cc1993547
Quellennotizuspto-grants-1986_07