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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1019357Erstellt: 26. Oktober 2026

Methanol → N-Allyl-N,N-di-n-octylamine

https://huagongshe.com/reaction/1019357

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDioctylamineHCID 3094—
EduktAllyl bromideHCID 7841—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-Allyl-N,N-di-n-octylamineHCID 4562804—

Reaktionsschritte

Vinylsulfomethylpolystyrene resin 3 (0.42 mmol g−1 (est), 160 mg) in DMF (2 cm3) was treated with dioctylamine (1.7 mmol, 515 mm3) at 20° C. for 24 h. The resin was washed with DMF (10×5 cm3) and DCM (10 cm3), resuspended in DMF (2 cm3) and treated with allyl bromide (4.25 mmol, 365 mm3) at 20° C. for 24 h. The solvent and the reagent was then removed by filtration and the resin washed with DCM (2×20 cm3). The elimination was performed in DCM (4 cm3) with DIEA (1.72 mmol, 300 mm3) overnight. The filtrate of this last reaction step was combined with the DCM and MeOH, washed (25 cm3) from the resin and evaporated. It gave 14 contaminated with DIEA in 38 mg yield. The amine was transferred in a little DCM (<5 cm3) to a K2CO3 covered dry silica column (5 g). Impurities were washed away with hexane and the amine eluted with ethyl acetate. After the removal of the solvent 14 was obtained as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06486354B1
Quelldatensatzuspto-grants-2002_11
ORD IDord-16cd478fae0741f69f5e2b4551b2edea
Quellennotizuspto-grants-2002_11