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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1632862Erstellt: 27. Oktober 2026

Hydrochloric Acid → 1-(2-Formamidophenyl)-1'-methylspiro[indoline-3,4'-piperidine] hydrochloride

https://huagongshe.com/reaction/1632862

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium MethoxideHCID 10942334—
Edukt1-(2-Aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine]dihydrochlorideHCID 12801598—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(2-Formamidophenyl)-1'-methylspiro[indoline-3,4'-piperidine] hydrochlorideHCID 12801604—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a mixture of 15.0 g of 1-(2-aminophenyl)-1'-methylspiro[indoline-3,4'-piperidine] dihydrochloride, Example 16, in 75 ml of dimethylformamide at 90° C. under nitrogen is added 8.6 g of sodium methoxide. Following this addition the reaction temperature is increased to 110°-115° C. and maintained at this temperature for 40 minutes. The resulting dark brown mixture is permitted to cool to 90° C. and then poured onto 800 ml of ice-water. The mixture is filtered and the filter cake is washed with water and then dissolved in chloroform. The chloroform solution is successively washed with brine, dried and concentrated leaving a red colored glass. The glass is dissolved in ether, where it is converted to its hydrochloric acid salt which is collected by filtration and then washed with ether and finally dried. The salt is recrystallized from a methyl alcohol-ether mixture to provide the product, mp 287.5° C., dec of 1-(2-formamidophenyl)-1'-methylspiro[indoline-3,4'-piperidine] hydrochloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04477667
Quelldatensatzuspto-grants-1984_10
ORD IDord-9fcb1c40465a43649cd770f9faf75304
Quellennotizuspto-grants-1984_10