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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 486487Erstellt: 24. Oktober 2026

Acetonitrile → Methyl (RS)-4-cyano-2-phenylbutanoate

https://huagongshe.com/de/reaction/486487

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktAmmonium ChlorideHCID 25517—
EduktMethyl atropateHCID 193334—
EduktLithium diisopropylamideHCID 2724682—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelCyclohexaneHCID 8078—
ProduktMethyl (RS)-4-cyano-2-phenylbutanoateHCID 5364509475%

Reaktionsschritte

Lithium diisopropylamide (3.67 ml of a 1.5 molar solution in cyclohexane) was added to acetonitrile (0.26 ml) in tetrahydrofuran (10 ml) at -78° C. After 1 hour, methyl 2-phenyl-acrylate (see Preparation 22) (0.81 g) in tetrahydrofurn (10 ml) was added and the mixture was stirred for 1 hour, allowed to warm to room temperature then treated with saturated ammonium chloride solution. The resulting mixture was partitioned between ethyl acetate and water, the organic phase dried over magnesium sulphate and evaporated to give a residue which was partitioned between ether and 10% aqueous sodium carbonate. The organic layer was dried over magnesium sulphate and evaporated to leave the title compound (0.5 g, 75%) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05292749
Quelldatensatzuspto-grants-1994_03
ORD IDord-80af75f55504407f8422051aeb00f6fc
Quellennotizuspto-grants-1994_03