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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1915987Erstellt: 25. Oktober 2026

Triethylamine → N-(4-hydroxy-3-methoxybenzyl)-4-methyl-1,2-dithiolane-4-carboxamide

https://huagongshe.com/reaction/1915987

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPhenol, 4-(aminomethyl)-2-methoxy-, hydrochloride (1:1)HCID 165576—
Edukt1-{[(4-Methyl-1,2-dithiolan-4-yl)carbonyl]oxy}pyrrolidine-2,5-dioneHCID 57505403—
Lösungsmittel2-MethyltetrahydrofuranHCID 7301—
ProduktN-(4-hydroxy-3-methoxybenzyl)-4-methyl-1,2-dithiolane-4-carboxamideHCID 45111293—

Reaktionsschritte

24.3 mmol of N-hydroxysuccinimide are added to 24.3 mmol of dithiolane acid dissolved in 60 ml of dichloromethane cooled to 0° C. (on an ice bath). The reaction medium is stirred for 30 minutes at 0° C. A solution of 24.3 mmol of DCC in 50 ml of dichloromethane is added and the mixture is then stirred at 20° C. for 4 hours. The reaction medium is filtered and washed, and the filtrate is then evaporated to dryness on a rotavapor at 40° C. under vacuum to give 1-{[(4-methyl-1,2-dithiolan-4-yl)carbonyl]oxy}pyrrolidine-2,5-dione (m=7 g, quantitative yield). 10 ml of MeTHF, 3.16 mmol of 4-(aminomethyl)-2-methoxyphenol hydrochloride and 3.16 mmol of triethylamine are added to 1.58 mmol of 1-{[(4-methyl-1,2-dithiolan-4-yl)carbonyl]oxy}pyrrolidine-2,5-dione. After stirring overnight, the mixture is filtered, rinsed with MeTHF and then evaporated. Flash chromatography, eluting with 98/2 dichloromethane/methanol, gives Compound 16 in the form of a yellow oil (84% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08617524B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-45a6fdd71c6f4f7b8e63beade604f60f
Quellennotizuspto-grants-2013_12