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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 400644Erstellt: 24. Oktober 2026

Allyl bromide → 2-Methyl-2-phenylpent-4-enenitrile

https://huagongshe.com/de/reaction/400644

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
Edukt2-PhenylpropionitrileHCID 15761—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelAmmonium ChlorideHCID 25517—
Produkt2-Methyl-2-phenylpent-4-enenitrileHCID 1051137999,6%

Reaktionsschritte

To a solution of 2-phenylpropionitrile (4.04 g, 30.79 mmol) in 40 mL of DMSO was added 34 mL (34 mmol) of a 1 M solution of sodium bis(trimethylsilyl)amide (NaHMDS) in THF over a 5 minute period. After 10 minutes, allyl bromide (6 mL, 69.33 mmol) was added dropwise (exothermic). The mixture was cooled with an ice-water bath. The mixture stirred for 20 minutes, becoming a solid mass. An additional 20 mL of DMSO was added. After 10 minutes, the mixture was diluted with 200 mL of ammonium chloride and extracted with three 100 mL portions of ethyl acetate. The combined organic layers were washed with six 75 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 5.25 g (99.5% yield) of 2-methyl-2-phenylpent-4-enenitrile as yellow oil which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741897B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-92b51de5a53942ec8f909e4ba5bb9eaf
Quellennotizuspto-grants-2014_06