HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743183Generated: October 26, 2026
Methyl iodide → 4-Methyl-2-[2-(4-phenylbutyl)phenoxymethyl]morpholine
https://huagongshe.com/reaction/743183
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-t-Butoxycarbonyl-2-[2-(4-phenylbutyl)phenoxymethyl]morpholine | HCID 10693685 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-Methyl-2-[2-(4-phenylbutyl)phenoxymethyl]morpholine | HCID 10809500 | 76.5% |
Reaction Steps
115 mg of potassium carbonate and 118 mg of methyl iodide were added to a solution of 300 mg of 2-[2-(4-phenylbutyl)phenoxymethyl]morpholine hydrochloride (prepared as described in Example 7) in 6 ml of dimethylacetamide, and the resulting mixture was allowed to react at room temperature for 3 hours. At the end of this time, the reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The resulting yellow oily residue was purified by column chromatography through silica gel, using ethyl acetate as the eluent, to give 183 mg (yield 65%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05556864 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-3cb7bf77cebc478abf0a594f12b794e2 |
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| Source note | uspto-grants-1996_09 |
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