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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1903592Erstellt: 24. Oktober 2026

Iodine → p-Chloroprenylbenzene

https://huagongshe.com/de/reaction/1903592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktEthyl BromideHCID 6332—
Eduktp-BromochlorobenzeneHCID 7806—
Edukt1-Chloro-3-methyl-2-buteneHCID 10429—
EduktAmmonium ChlorideHCID 25517—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produktp-ChloroprenylbenzeneHCID 31646064%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

Under nitrogen atmosphere, 55.1 g of magnesium turnings, 800 ml of tetrahydrofuran, and about 0.1 g of several pieces of iodine were put in a flask. With stirring, 2 ml of ethyl bromide was added, whereupon coloration by iodine disappeared. Then, a solution of 361.7 g of p-bromochlorobenzene in 2 liters of tetrahydrofuran was added dropwise at such a speed that the reaction temperature was maintained at 25° C. to 30° C. After the addition, the mixture was further stirred for 1 hour, and cooled to about 20° C. A solution of 256.8 g of prenyl chloride in 800 ml of tetrahydrofuran was added dropwise at 15° C. to 20° C. over the course of about 4 hours. After the addition, the mixture was left to stand overnight at room temperature. Two liters of a 10% by weight aqueous solution of ammonium chloride were added, and the mixture was separated into an organic layer and an aqueous layer. The aqueous layer was extracted with 300 ml of diethyl ether. The diethyl ether layer was combined with the organic layer previously separated, and washed with water, dried, concentrated, and distilled to give 218.3 g (yield 64.0%) of p-chloroprenylbenzene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04436939
Quelldatensatzuspto-grants-1984_03
ORD IDord-e845d51c3bf74f8088a6672306956ca5
Quellennotizuspto-grants-1984_03