Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Reactant | 4-Benzyl-2-toluene-p-sulphonyloxymethylmorpholine | HCID 12297767 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21519218 | HCID 21519218 | — |
Reaction Steps
A mixture of 3-methoxyaniline (12.5 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-(3-methoxyanilino)methylmorpholine toluene-p-sulphonate, m.p. 102-103°C. The toluene-p-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-(3-methoxyanilino)methylmorpholine dihydrochloride monohydrate melts at 116-118°C. after crystallisation from methanol/ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03974156 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-7d1da896756e4d32bde7f12d0bf50ea1 |
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| Source note | uspto-grants-1976_08 |
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