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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1388803Erstellt: 27. Oktober 2026

Ethyl Bromide → Ethyl alpha-[p-(3-methyl-2-butenyl)phenyl]propionate

https://huagongshe.com/reaction/1388803

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 2-bromopropionateHCID 79040—
Eduktp-ChloroprenylbenzeneHCID 316460—
EduktMagnesiumHCID 5462224—
KatalysatorNickel DichlorideHCID 24385—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl alpha-[p-(3-methyl-2-butenyl)phenyl]propionateHCID 1311808349,1%

Reaktionsschritte

Under a nitrogen atmosphere, 0.3 ml of ethyl bromide was added to a mixture of 0.97 g of magnesium turning for Grignard reaction and 2 ml of THF. After the starting of the reaction, a solution composed of 6.01 g of p-chloroprenylbenzene and 1 ml of THF was added dropwise while maintaining the temperature at 115° to 130° C. After the addition, THF was added further as required, and the mixture was stirred at 110° to 120° C. for 4 hours. After cooling, 20 ml of THF was further added, and the resulting reaction mixture was added dropwise to a solution composed of 5.43 g of ethyl α-bromopropionate, 0.016 g of nickel chloride and 5 ml of THF. After the addition, the mixture was further stirred for 1 hour, and an aqueous solution of ammonium chloride was added. The mixture was extracted with diethyl ether. The ethereal extract was washed with an aqueous solution of sodium chloride, dried, concentrated and distilled to give 3.62 g (yield 49.1%) of ethyl α-(p-prenylphenyl)propionate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04433160
Quelldatensatzuspto-grants-1984_02
ORD IDord-df554f621f6543b3aff215019144c817
Quellennotizuspto-grants-1984_02