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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1375307Erstellt: 25. Oktober 2026

Iodoethane → N-Ethylphenothiazine

https://huagongshe.com/reaction/1375307

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 (from Fluka), 11.7 g (0.075 mol) of iodoethane (from Aldrich), 4.2 g (0.075 mol) of potassium hydroxide, and 0.25 g of tetra-n-butylammonium hydrogen sulfate (from Aldrich) in 200 ml of dry toluene was refluxed for 24 hrs. The cooled reaction mixture was filtered and the solvent was evaporated. The product was recrystallized from methanol. The yield of 10-ethylphenothiazine was 10.2 g (90%). The product had a melting point of 103–104° C. (recrystallized from methanol). A 1H NMR spectrum yielded the following results (100 MHz, CDCl3, 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
PatentnummerUS07169520B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-243b4f4bd18e4e9b86c3f72c39e5d38d
Quellennotizuspto-grants-2007_01