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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1375308Erstellt: 26. Oktober 2026

Dimethylformamide → 10-Ethylphenothiazine-3-carbaldehyde

https://huagongshe.com/reaction/1375308

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium HydroxideHCID 14797—
EduktPhosphorus oxychlorideHCID 24813—
EduktN-EthylphenothiazineHCID 219178—
Produkt10-Ethylphenothiazine-3-carbaldehydeHCID 314330—

Reaktionsschritte

A 3.7 ml (0.04 mol) quantity of phosphorus oxychloride (from Aldrich) was added dropwise to 4.4 ml (0.06 mol) of dry dimethylformamide (DMF) at 0° C. under a nitrogen atmosphere. This solution was warmed up slowly to room temperature. Then 5 g (0.02 mol) of 10-ethylphenothiazine in dry DMF was added dropwise to the solution. The reaction mixture was heated at 80° C. for 24 hours and poured into ice water. The obtained solution was neutralized with potassium hydroxide until the pH reached 6–8. The product was extracted with chloroform. The chloroform extract was dried with anhydrous sodium sulfate, filtered and distilled. The product was recrystallized from methanol. The yield of 10-ethylphenothiazine-3-carbaldehyde was 3.7 g (66%). The product had a melting point of 94–95° C. (recrystallized from methanol). A 1H NMR spectrum yielded the following results: (100 MHz, CDCl3, δ, ppm): 1.50 (t, J=7.0 Hz, 3H, CH3); 4.02 (q, J=7.0 Hz, 2H, CH2); 6.95–6.39 (m, 5H, Ar), 7.52–7.70 (m, 2H, Ar), 9.83 (s, 1H, CHO).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07169520B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-47241199647d4ce089373cf99779e30a
Quellennotizuspto-grants-2007_01