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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 437181생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/437181

반응식

참여 물질

역할이름HCID투입량
반응물o-PhenetidineHCID 7203—
반응물4-Benzyl-2-toluene-p-sulphonyloxymethylmorpholineHCID 12297767—
용매Diethyl EtherHCID 3283—
생성물4-Benzyl-2-(2-ethoxyanilino)methylmorpholine toluene-p-sulphonateHCID 21430390—

반응 조건

온도95 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04029786
출처 데이터셋uspto-grants-1977_06
ORD IDord-d7512c75706848f79c8959a5584299b7
출처 메모uspto-grants-1977_06