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HRID 437181作成日:2026年10月26日

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

https://huagongshe.com/reaction/437181

反応式

関与物質

役割名称HCID仕込み量
反応物o-PhenetidineHCID 7203—
反応物4-Benzyl-2-toluene-p-sulphonyloxymethylmorpholineHCID 12297767—
溶媒Diethyl EtherHCID 3283—
生成物4-Benzyl-2-(2-ethoxyanilino)methylmorpholine toluene-p-sulphonateHCID 21430390—

反応条件

温度95 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04029786
出典データセットuspto-grants-1977_06
ORD IDord-d7512c75706848f79c8959a5584299b7
出典メモuspto-grants-1977_06