HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859444Generated: November 2, 2026
Sodium Iodide → (S)-3-(4-Nitrobenzoyloxy)-1-(4-methoxyphenethyl)pyrrolidine
https://huagongshe.com/reaction/1859444
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(4-Methoxyphenyl)ethyl 4-methylbenzenesulfonate | HCID 285384 | — |
| Reactant | (S)-3-(4-nitrobenzoyloxy)pyrrolidine | HCID 12148704 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-3-(4-Nitrobenzoyloxy)-1-(4-methoxyphenethyl)pyrrolidine | HCID 69901303 | — |
Reaction Steps
4-Methoxyphenethyl tosylate (1.24 g, 4.05 mmol), sodium carbonate (430 mg, 4.06 mmol) and sodium iodide (40 mg, 0.26 mmol) were added to a solution of (S)-3-(4-nitrobenzoyloxy)pyrrolidine (799 mg, 3.38 mmol) in acetonitrile (40 ml), and they were heated under reflux at 90° C. for 3 hours. The insoluble material was removed by the filtration. The insoluble material was washed with ethyl acetate, and the wash solution was combined with the filtrate. The solvent was evaporated under reduced pressure. The obtained residue was subjected to silica gel column chromatography. The product was eluted with hexane and ethyl acetate (10:1) and then with a mixture of the same solvents (1:1). The appropriate fractions were combined, and the solvent was evaporated under reduced pressure to obtain (S)-3-(4-nitrobenzoyloxy)-1-(4-methoxy-phenethyl)pyrrolidine in the form of a light yellow oil (1.00 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06528504B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-aaf43faa9e074a3eba372d6a44c7e83b |
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| Source note | uspto-grants-2003_03 |
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