Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 67137822 | HCID 67137822 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67136588 | HCID 67136588 | 73% |
Reaction Steps
Tetra-n-butylammonium bromide (380 mg, 1.18 mmol) and ethyl iodide (0.4 ml, 5.0 mmol) were added to a solution of 1-{3-(tert-butyl)-5-[(3S,4S)-3-hydroxy-4-(methoxymethoxy)tetrahydro-1H-1-pyrrolyl]-4-methoxyphenyl}-1-ethanone (830 mg, 2.36 mmol) in a toluene (5 ml) −50% aqueous NaOH (5 ml) mixed solvent at room temperature in that order and the mixture was stirred for 19 hours. After further adding ethyl iodide (0.2 ml) and stirring for 9 hours, more ethyl iodide (0.2 ml) was added and stirring was continued for 60 hours. The mixture was diluted with water, extraction was performed with ethyl acetate and the extract was washed with brine. After drying with anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (650 mg, 73%) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244730B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-f7bb3cf36969457f98076c09529d9fcd |
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| Source note | uspto-grants-2007_07 |
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