Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22153Erstellt: 24. Oktober 2026

Hydrochloric Acid → Tert-butoxycarbonyl-N,N'-dimethyl hexane diamine

https://huagongshe.com/de/reaction/22153

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiethyl EtherHCID 3283—
EduktCarbonazidic acid, 1,1-dimethylethyl esterHCID 61256—
EduktN,N'-dimethyl-hexanediamineHCID 22571325—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
ProduktTert-butoxycarbonyl-N,N'-dimethyl hexane diamineHCID 19927281—

Reaktionsschritte

Tert-butoxycarbonyl azide in ether ("Organic Synthesis V", p. 157-158) (2.9 g, 20 mmol, 5.2 ml) was added dropwise to a stirred solution of N,N'-dimethyl-hexane diamine (Aldrich Cat. No. D16110-1) (Beilstein 4(1), p. 422) (2.92 g, 20 mmol) in dimethyl sulphoxide (DMSO) (30 ml). The temperature was kept at 20° C. with external cooling. After the addition was complete (30 minutes), stirring was continued at room temperature for 1 hour, whereupon water (30 ml) was added. The solution was acidified (pH 5) with 2N HCl and extracted with ether (2 ×200 ml). The DMSO/water-mixture was made alkaline (pH 11) with 6N NaOH and extracted with ether (4×200 ml). Evaporation of the ether gave the title compound (1) (1.2 g) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05427779
Quelldatensatzuspto-grants-1995_06
ORD IDord-4f37d6077a094a768fe4bf681ddb179d
Quellennotizuspto-grants-1995_06