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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 437181Erstellt: 24. Oktober 2026

o-Phenetidine → 4-Benzyl-2-(2-ethoxyanilino)methylmorpholine toluene-p-sulphonate

https://huagongshe.com/de/reaction/437181

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukto-PhenetidineHCID 7203—
Edukt4-Benzyl-2-toluene-p-sulphonyloxymethylmorpholineHCID 12297767—
LösungsmittelDiethyl EtherHCID 3283—
Produkt4-Benzyl-2-(2-ethoxyanilino)methylmorpholine toluene-p-sulphonateHCID 21430390—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A mixture of 2-ethoxyaniline (14.0 g.) and 4-benzyl-2-toluene-p-sulphonyloxymethylmorpholine (18.6 g.) is stirred and heated on the steam bath (95° C.) under nitrogen for 24 hours. The mixture is cooled and ether added. The solid thus obtained is collected and crystallised from ethyl acetate to give 4-benzyl-2-(2-ethoxyanilino)methylmorpholine toluene-p-sulphonate, m.p. 127° C. The toluene sulphonate salt is converted into the corresponding dihydrochloride by basifying it with dilute sodium hydroxide solution, extracting the base into ether (3× 200 ml.), washing the ethereal extract with water and then drying it over anhydrous magnesium sulphate followed by filtration and treatment of the ethereal solution of base with ethereal hydrochloric acid solution. The 4-benzyl-2-(2-ethoxyanilino)-methylmorpholine dihydrochloride melts at 226° C. after crystallisation from methanol/ethyl acetate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04029786
Quelldatensatzuspto-grants-1977_06
ORD IDord-d7512c75706848f79c8959a5584299b7
Quellennotizuspto-grants-1977_06