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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283096Generated: October 27, 2026

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

https://huagongshe.com/reaction/1283096

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-PhenetidineHCID 7203—
Reactant4-Benzyl-2-toluene-p-sulphonyloxymethylmorpholineHCID 12297767—
SolventDiethyl EtherHCID 3283—
Product4-Benzyl-2-(2-ethoxyanilino)methylmorpholine toluene-p-sulphonateHCID 21430390—

Reaction Conditions

Temperature95 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03974158
Source datasetuspto-grants-1976_08
ORD IDord-aa2bd4fd26c64a518a34e58eba5a78c1
Source noteuspto-grants-1976_08