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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374666Erstellt: 24. Oktober 2026

Diisopropylamine → N,N-Diisopropylmethallylamine

https://huagongshe.com/de/reaction/374666

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktAdiponitrileHCID 8128—
Edukt3-Chloro-2-methyl-1-propeneHCID 11241—
EduktPotassium HydroxideHCID 14797—
KatalysatorTetrabutylammonium IodideHCID 67553—
ProduktN,N-DiisopropylmethallylamineHCID 18997629—

Reaktionsschritte

A mixture of diisopropylamine (20.24 g, 0.2 mol), methallyl chloride (9.00 g, 0.1 mol), adiponitrile (10.81 g, 0.1 mol) and tetrabutylammonium iodide (3.69 g, 10 mmol) was refluxed for 5 h with vigorous stirring (two phases). The temperature of the mixture increased from 88° to 125° C. Potassium hydroxide solution (5M, 15 ml, 0.15 mol) was added. Three layers formed. The mixture was extracted with n-pentane (2×50 ml). Adiponitrile (the middle layer) was recovered. The pentane solution was dried with anhydrous magnesium sulfate and the product was isolated by distillation: 12.58 g (81%), bp 75-77° C/45 mm Hg. 1H NMR CDCl3 δ ppm, 0.98 (d, J=6.6 Hz, 12H, CH3), 1.70 (s, 3H, CH3), 2.97 (m, 4H, CH2, CH), 4.78 (s, 1H,=CH2), 4.93 (m, 1H,=CH2) .

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05481038
Quelldatensatzuspto-grants-1996_01
ORD IDord-fb65b72582d243408b7a07a8172ce6f8
Quellennotizuspto-grants-1996_01