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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277689Erstellt: 24. Oktober 2026

Tert-Butylbenzene → HCID 22625489, Verbindung

https://huagongshe.com/de/reaction/277689

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-ButylbenzeneHCID 7366—
EduktIodosylbenzeneHCID 92125—
Edukt1-Propanesulfonic acid, 1,1,2,3,3,3-hexafluoro-HCID 9794628—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 22625489HCID 22625489—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4.4 g (20 mmol) of iodosylbenzene was suspended in 100 ml of dry dichloromethane. The suspension was cooled to 0° C. with stirring. 4.65 g (20 mmol) of 3,3,3,2,1,1-hexafluoropropane sulfonic acid (optionally distilled) was added at the same temperature thereto under exclusion of moisture. The mixture was stirred at room temperature for 3 hours. The temperature of the mixture was returned to 0° C., and 2.68 g (20 mmol) of 4-t-butylbenzene was added thereto at that temperature. The temperature of the mixture was returned to room temperature, followed by stirring for 6 hours. Thereafter, the insolubles were removed by filtration. The solvent was removed from the filtrate. The oily residue was purified by recrystallization (twice) from diethyl ether. The structure was confirmed by 1H-NMR (CDCl3): δ=0.81 (s, 9H), 4.98-5.22 (m[d], 1H), 7.18-7.23 (d, 2H), 7.58-7.65 ppm (m, 7H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358665B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-10b1fad91dc64ce68db68fd3e18524a1
Quellennotizuspto-grants-2002_03