Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-methyl-4-nitrophenethylamine | HCID 2794239 | — |
| Reactant | HCID 20086989 | HCID 20086989 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19915717 | HCID 19915717 | 38.1% |
Reaction Steps
A suspension of N-methyl-4-nitrophenethylamine (1.1 g), 2-(4-methanesulphonamidophenoxy)ethyl chloride (1.5 g), sodium bicarbonate (0.5 g) and sodium iodide (0.9 g) in acetonitrile (100 ml) was stirred at reflux for 4 days. On evaporation to dryness the resultant oil was partitioned between 2N aqueous sodium bicarbonate solution and methylene chloride. After two further extractions with methylene chloride, the organic portions were combined, washed with saturated brine solution, dried over anhydrous magnesium sulphate, filtered and evaporated to dryness. The resultant brown oil was chromatographed on silica ("Kieselgel 60"--Trade Mark) eluting with ethyl acetate followed by collection and evaporation of suitable fractions to give the title compound as a yellow solid, (0.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05079248 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-9c7d2b8325c745c3b1ebf6d2a35c0572 |
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| Source note | uspto-grants-1992_01 |
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