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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 267917Erstellt: 26. Oktober 2026

Potassium Hydroxide → 9,9-Dimethyl-10-[5-methyl-1-(5-methyl-1-pyrrolin-2-YL)-2-pyrrolin-2-YL]acridan

https://huagongshe.com/reaction/267917

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt9,9-Dimethyl-9,10-dihydroacridineHCID 22647—
EduktPhosphorus oxychlorideHCID 24813—
Edukt5-Methyl-2-pyrrolidoneHCID 66055—
Edukt9,9-Dimethyl-10-[5-methyl-1-(5-methyl-1-pyrrolin-2-YL)-2-pyrrolin-2-YL]acridan hydrochlorideHCID 20307164—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt9,9-Dimethyl-10-[5-methyl-1-(5-methyl-1-pyrrolin-2-YL)-2-pyrrolin-2-YL]acridanHCID 1279940035%

Reaktionsschritte

A mixture of 5-methyl-2-pyrrolidinone (2.0 g., 0.02 mole) and phosphorus oxychloride (3.0 g., 0.02 mole) in 15 ml. of 1,2-dichloroethane after standing 15 hr. at room temperature is combined with 9,9-dimethylacridan (2.1 g., 0.01 mole) after a 48 hr. period is added to 30 ml. of 5N potassium hydroxide and 30 g. of crushed ice. The 1,2-dichloroethane fraction is separated, extracted with 50 ml. of 1.5N hydrochloric acid and 50 ml. of water and dried over magnesium sulfate. Concentration of the 1,2-dichloroethane solution provides a residue which is stirred with 100 ml. of ether and filtered. The filter cake containing crude hydrochloride salt of the product is stirred with sodium hydroxide solution affording the free base. Crystallization from n-heptane provides 1.3 g. (35% yield) of 9,9-DIMETHYL-10-[5-METHYL-1-(5-METHYL-1-PYRROLIN-2-YL)-2-PYRROLIN-2-YL]ACRIDAN, m.p. 135°-139° C. from which the hydrochloride salt is prepared according to the procedure of Example 1. Analytically pure 9,9-DIMETHYL-10-[5-METHYL-1-(5-METHYL-1 -PYRROLIN-2-YL)-2-PYRROLIN-2-YL]ACRIDAN HYDROCHLORIDE, from acetone-ether, has a melting point of 247.5°-248.0° C. (corr.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03946004
Quelldatensatzuspto-grants-1976_03
ORD IDord-8dc6e2392f35482f976259e0a8a9a04c
Quellennotizuspto-grants-1976_03