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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 267915Erstellt: 26. Oktober 2026

1,2-Dichloroethane → HCID 178423700, Verbindung

https://huagongshe.com/reaction/267915

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktPhenothiazineHCID 7108—
EduktPotassium HydroxideHCID 14797—
EduktPhosphorus oxychlorideHCID 24813—
Edukt5-Methyl-2-pyrrolidoneHCID 66055—
ProduktHCID 178423700HCID 17842370017%

Reaktionsschritte

A mixture of 5-methyl-2-pyrrolidinone (6.0 g., 0.06 mole), phosphorus oxychloride (9.2 g., 0.06 mole) in 60 ml. of 1,2-dichloroethane is refluxed for 10 min. A solution of phenothiazine (6.0 g., 0.03 mole) in 20 ml. of 1,2-dichloroethane is added at the end of the reflux period and the reaction mixture stirred and refluxed for 20 hr., and then poured onto 20 ml. of 5N potassium hydroxide and 20 g. of crushed ice. The 1,2-dichloroethane layer is separated and extracted with 30 ml. of 1.5N hydrochloric acid and 30 ml. of water removing water soluble by-product 10-[2-(5-methyl-1-pyrrolinyl)]-phenothiazine hydrochloride. After drying the 1,2-dichloroethane solution over magnesium sulfate, the 1,2-dichloroethane solution is concentrated and the solid thus obtained stirred with 40 ml. of acetone and filtered. Crystallization of the filtercake from ethanol-ether provides analytically pure 10-[5-METHYL-1-(5-METHYL-1 -PYRROLIN-2-YL]PHENOTHIAZINE HYDROCHLORIDE in a yield of 17%, m.p. 257°-264° C. (corr.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03946004
Quelldatensatzuspto-grants-1976_03
ORD IDord-be28f5f9e3d545928b4392e148b1dfae
Quellennotizuspto-grants-1976_03