HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5074Generated: October 25, 2026
Hydrochloric Acid → (2S, 4S)-4-(4-methoxybenzylthio)-2-methylcarbamoylpyrrolidine
https://huagongshe.com/reaction/5074
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2S, 4S)-1-(t-Butoxycarbonyl)-4-(4-methoxybenzyl-thio)-2-methylcarbamoylpyrrolidine | HCID 57062218 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2S, 4S)-4-(4-methoxybenzylthio)-2-methylcarbamoylpyrrolidine | HCID 14880277 | 79.4% |
Reaction Steps
52.5 ml of a 4N dioxane solution of hydrogen chloride were added, whilst ice-cooling, to a solution of 4.00 g of (2S, 4S)-1-(t-butoxycarbonyl)-4-(4-methoxybenzylthio)-2-methylcarbamoylpyrrolidine [prepared as described in step (3) above] dissolved in 50 ml of ethyl acetate. The mixture was stirred at 0° to 50° C. for 30 minutes and then at room temperature for 2 hours. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate to make it weakly basic, and it was then extracted with ethyl acetate. The aqueous layer was saturated with ammonium chloride and then extracted with tetrahydrofuran. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel (eluted with a 5:1 mixture by volume of ethyl acetate and methanol), to afford 2.34 g of the title compound as colorless crystals, melting at 53°-54° C.
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-0e70b857ff5341b6b9e0f7b265b239d3 |
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| Source note | uspto-grants-1993_09 |
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