HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5084Generated: October 30, 2026
Methyl iodide → (2S, 4S)-4-(4-methoxybenzylthio)-2-methoxycarbonyl-1-methylpyrrolidine
https://huagongshe.com/reaction/5084
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2S, 4S)-4-(4-Methoxybenzylthio)-2-methoxycarbonylpyrrolidine | HCID 15200411 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2S, 4S)-4-(4-methoxybenzylthio)-2-methoxycarbonyl-1-methylpyrrolidine | HCID 57321322 | 27.9% |
Reaction Steps
1.18 g of sodium bicarbonate and 0.876 ml of methyl iodide were added, whilst ice-cooling, to a solution of 3.3 g of (2S, 4S)-4-(4-methoxybenzylthio)-2-methoxycarbonylpyrrolidine [prepared as described in step (9) above] dissolved in 30 ml of dry dimethylformamide, and the mixture was stirred at room temperature for 5 hours. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate and extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography over silica gel (eluted with a 1:2 by volume mixture of ethyl acetate and benzene), to afford 968 mg of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05242914 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-2d65ae8fa14242fd82d46e52981a6b6d |
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| Source note | uspto-grants-1993_09 |
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