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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 435425Erstellt: 24. Oktober 2026

Diisopropylamine → 4-p-Tolylsulfonyl-4,3,3,-trimethyl-pentanenitrile

https://huagongshe.com/de/reaction/435425

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktCyclohexaneHCID 8078—
Edukt3-Methyl-2-butenenitrileHCID 94301—
Edukt1-(Isopropylsulfonyl)-4-methylbenzeneHCID 816792—
EduktMonosodium phosphateHCID 23672064—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-p-Tolylsulfonyl-4,3,3,-trimethyl-pentanenitrileHCID 12833028—

Reaktionsschritte

3.81 ml of a cyclohexane solution of 1.75M of butyllithium were added at -30° to -40° C. to a mixture of 1.05 ml of diisopropylamine and 4 ml of tetrahydrofuran and the mixture was stirred for 10 minutes and was then cooled to -60° to -70° C. Then 1.22 g of p-tolyl isopropylsulfone were added to the mixture which after 15 minutes of contact was poured over 10 minutes under an inert atmosphere into a solution of 0.5 g of dimethylacrylonitrile and 4 ml of tetrahydrofuran at -60° to -70° C. The mixture was stirred for 30 minutes at -60° to -70° C. and was then poured into an aqueous saturated monosodium phosphate solution. The mixture was extracted with benzene and the organic phase was dried and evaporated to dryness. The residue was crystallized from isopropyl ether to obtain 0.740 g of 4-p-tolylsulfonyl-4,3,3,-trimethyl-pentanenitrile melting at 126° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04401601
Quelldatensatzuspto-grants-1983_08
ORD IDord-65212fa3874a4fbfb05ef8243326a26e
Quellennotizuspto-grants-1983_08