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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11202Erstellt: 23. Oktober 2026

Methanol → N-[3-(1,3-dioxolyl)phenyl]isatin

https://huagongshe.com/de/reaction/11202

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktIsatinHCID 7054—
EduktSodium hydrideHCID 24758—
Edukt2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelChloroformHCID 6212—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[3-(1,3-dioxolyl)phenyl]isatinHCID 21972258—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Isatin (3.2 g, 0.0218 mol) was dissolved in anhydrous DMF (75 ml) and cooled in an ice-bath under a nitrogen atmosphere. To this cold solution, sodium hydride (0.575 g, 0.0239 mol) was added and the reaction was stirred at 0° C. for 1.5 hours. This solution was then treated with 2-(3-bromophenyl)-1,3-dioxolane (5 g, 1 equivalent) followed by CuI (8.3 g, 2 equivalents). The resulting suspension was heated in an oil-bath under nitrogen at 130–140° C. for 16 hours. It was then cooled to room temperature and diluted with an equal volume of chloroform. This suspension was filtered and the filtrate was concentrated under reduced pressure. A viscous brown oil was recovered which was suspended in xylenes (150 ml) wand evaporated to dryness. The residue was used as such for the next reaction. TLC (5% methanol in chloroform) showed clean conversion; Rf (product)=0.86.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07097995B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-0e3a377f9f97467ab5412975fa58ae7c
Quellennotizuspto-grants-2006_08