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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 653694Erstellt: 25. Oktober 2026

Triethylamine → N-(2,3-dimethylnaphthyl)-N-(2-oxo-tetrahydrofuran-3-yl)-N-(2-methoxy-ethoxy-acetyl)-amine

https://huagongshe.com/reaction/653694

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-(2-Methoxyethoxy)acetyl chlorideHCID 7010338—
EduktN-(2,3-dimethylnaphtyl)-N-(2-oxo-tetrahydrofuran-3-yl)-amineHCID 13092367—
LösungsmittelTolueneHCID 1140—
ProduktN-(2,3-dimethylnaphthyl)-N-(2-oxo-tetrahydrofuran-3-yl)-N-(2-methoxy-ethoxy-acetyl)-amineHCID 67917313—

Reaktionsschritte

To 15.3 g of N-(2,3-dimethylnaphtyl)-N-(2-oxo-tetrahydrofuran-3-yl)-amine in 120 ml of toluene are added dropwise 12.2 g of 2-methoxyethoxy-acetyl chloride (MAC) in 20 ml of toluene and afterwards 8.1 g of triethylamine in 20 ml of toluene. The temperature of the reaction rises to 35° and is then raised to 40° for 2 hours. There are subsequently added dropwise a further 2 g of MAC and 1.5 g of triethylamine. The temperature is held overnight at 40°, and afterwards a further 2 g of MAC are added dropwise. After 4 hours, the reaction mixture is cooled to room temperature and filtered, and the filtrate is concentrated by evaporation to yield a resinous residue, which is purified through silica gel 60 using ethyl acetate as the eluant. The solid product occurring from the residue is recrystallised from isopropanol with the addition of active charcoal. The resulting product is the colourless diastereoisomeric mixture of the compound No. 32, m.p. 142°-146°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05128371
Quelldatensatzuspto-grants-1992_07
ORD IDord-c433676cfe3a49bcbd1730250bdf12da
Quellennotizuspto-grants-1992_07