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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 497065Erstellt: 24. Oktober 2026

Toluene → N-[2-(1-methylpyrrolidin-2-yl)ethyl]caprylamide

https://huagongshe.com/de/reaction/497065

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktEthyl octanoateHCID 7799—
EduktSodium HydroxideHCID 14798—
Edukt2-(2-Aminoethyl)-1-methylpyrrolidineHCID 98388—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-[2-(1-methylpyrrolidin-2-yl)ethyl]caprylamideHCID 989978874,5%

Reaktionsschritte

Toluene (1.0 ml), dried using MS 4A, was mixed with 1.48 ml of a n-hexane solution of 15% Me3Al. With the mixture being cooled in an ice-methanol bath, 0.25 ml (1.16 mmols) of 2-(2-aminoethyl)-1-methylpyrrolidine was added dropwise over about 2 minutes. After stirring for 20 minutes, the temperature was raised to room temperature, and 0.5 ml of a toluene solution of 0.2 g (1.16 mmols) of caprylic acid ethyl ester was added dropwise over 1 minute. After stirring for 2 hours at 70° C., the mixture was cooled with ice, and 10 ml of 1N NaOH was added dropwise. The mixture was stirred for 10 minutes, and water and ethyl acetate were added. Then, the mixture was separated into respective layers, and the organic layer was washed twice with 20 ml of a saturated aqueous solution of sodium chloride. After this layer was dried over anhydrous magnesium sulfate, it was concentrated under reduced pressure on a 30° C. water bath to obtain the captioned compound (yield 0.22 g). This compound was subjected to silica gel column chromatography (mobile phase: CHCl3:MeOH (19:1→9:1)) for purification. NMR and mass spectrum confirmed the purified compound to have the following structure:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06949553B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-b69df3b1618c4dad8dab15b02595d4a6
Quellennotizuspto-grants-2005_09