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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1646821Erstellt: 24. Oktober 2026

Water → 5-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrile

https://huagongshe.com/de/reaction/1646821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDiisopropyl EtherHCID 7914—
EduktSodium CyanideHCID 8929—
Edukt1-Iodo-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-4-phenylbutaneHCID 19088027—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt5-(2,5-Dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrileHCID 19088086163%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of 4.19 g (5.0 mmole) of 1-iodo-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-4-phenylbutane in dimethylsulfoxide (30 ml) was added 0.74 g (5×3 mmole) of sodium cyanide, and the mixture was stirred at 50° C. for 2 hours. The reaction solution was cooled with ice, and isopropyl ether and water were added to it, followed by stirring. The isopropyl ether layer was separated out, washed with aqueous sodium chloride solution, dried (magnesium sulfate) and evaporated. The residual solution was chromatographed on a silica gel column to perform purification (elution with isopropyl ether/hexane) to thereby give 1.65 g (98%) of 5-(2,5-dimethoxy-3,4,6-trimethylphenyl)-5-phenylvaleronitrile. Its typical physical properties and nuclear magnetic resonance spectrum data are shown in Table 14.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05180742
Quelldatensatzuspto-grants-1993_01
ORD IDord-073e1732a2dc4675b31c1d894df7e311
Quellennotizuspto-grants-1993_01