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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1067904Erstellt: 27. Oktober 2026

Diethyl Sulfate → tert-Butylisobutylethylamine

https://huagongshe.com/reaction/1067904

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl SulfateHCID 6163—
EduktHexaneHCID 8058—
EduktPotassium HydroxideHCID 14797—
EduktN-tert-butyl-2-methylpropan-1-amineHCID 527145—
EduktButyllithiumHCID 178418339—
Produkttert-ButylisobutylethylamineHCID 438494172%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A mixture of tert-butylisobutylamine (25.84 g, 0.2 mol) and diethyl sulfate (46.26 g, 0.3 mol) was warmed to 70° C. with stirring. An exothermic reaction started and in a few minutes the temperature rose to 150° C. with vigorous boiling of the mixture. After cooling to ˜50° C., 5 M aqueous potassium hydroxide (100 ml, 0.5 mol) was added. The organic layer was separated and dried over anhydrous magnesium sulfate. Diethyl sulfate (10 ml) was added and the mixture was stirred at 100° C. for 1 h. Aqueous 5 M potassium hydroxide (100 ml) was added and the mixture was stirred at 80° C. for 1 h. The organic layer was separated and the aqueous layer was extracted with diethyl ether (50 ml). The organic solutions were combined, dried over anhydrous magnesium sulfate and the product was isolated by distillation. A small amount (1-2%) of tert-butylisobutylamine which was removed by the addition of 2.5 M n-butyllithium in hexane (5.0 ml, 10 mmol) and the product distilled to yield 22.56 g, (72%) of product, bp 68-70° C./40 mm Hg; 1H NMR (CDCl3) δ0.85 (d, J=6.5 Hz, 6H, CH3), 0.98 (t, J=6.5 Hz, 3H, CH3), 1.01 (s, 9H, CH3), 1.66 (n, J=6.5 Hz, 1H, CH), 2.04 (d, J=6.57 Hz, 2H, CH2), 2.51 (q, J=6.5 Hz, 2H, CH2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06248885B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-34b25f9e93fc43feb5b9c968548cab3e
Quellennotizuspto-grants-2001_06