HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437181Generated: October 26, 2026
o-Phenetidine → 4-Benzyl-2-(2-ethoxyanilino)methylmorpholine toluene-p-sulphonate
https://huagongshe.com/reaction/437181
Participants
| Role | Name | HCID | Charge |
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| Reactant | o-Phenetidine | HCID 7203 | — |
| Reactant | 4-Benzyl-2-toluene-p-sulphonyloxymethylmorpholine | HCID 12297767 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Benzyl-2-(2-ethoxyanilino)methylmorpholine toluene-p-sulphonate | HCID 21430390 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04029786 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-d7512c75706848f79c8959a5584299b7 |
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| Source note | uspto-grants-1977_06 |
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