Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 268576Erstellt: 24. Oktober 2026

Iodoethane → N-Ethylphenothiazine

https://huagongshe.com/de/reaction/268576

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
EduktPhenothiazineHCID 7108—
EduktPotassium HydroxideHCID 14797—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelTolueneHCID 1140—
ProduktN-EthylphenothiazineHCID 219178—

Reaktionsschritte

A mixture of 10 g (0.05 mol) of phenothiazine (obtained from Fluka), 11.7 g (0.075 mol) of iodoethane (obtained from Aldrich), 4.2 g (0.075 mol) of potassium hydroxide and 0.25 g of tetra-n-butylammonium hydrogen sulfate (obtained from Aldrich) in 200 ml of dry toluene was refluxed for 24 hours. After cooling, the reaction mixture was filtered and the solvent was evaporated. The product was recrystallized from methanol. The yield of 10-ethylphenothiazine (C14H13NS, FW=227.33) was 90%. The melting point of the product was 103-104° C. The 1H-NMR spectrum (100 MHz) of the product in CDCl3 was characterized by the following chemical shifts (δ, ppm): 1.40 (t, J=7.0 Hz, 3H, CH3); 3.90 (q, J=7.0 Hz, 2H, CH2); 6.78-7.32 (m, 8H, Ar).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07445877B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-5dca1ffcee9c4e1fac40ef9667593d59
Quellennotizuspto-grants-2008_11