HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338828Generated: October 25, 2026
Hydrochloric Acid → HCID 51041670, compound
https://huagongshe.com/reaction/338828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Bis(trifluoroacetoxy)iodobenzene | HCID 102317 | — |
| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Reactant | (S)-benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylate | HCID 86707398 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 51041670 | HCID 51041670 | 93.2% |
Reaction Steps
To (S)-Benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylate (35.61 g, 135.8 mmol) in 1:1 MeCN/H2O (100 mL) was added [bis(trifluoroacetoxy)iodo]benzene (58.38 g, 135.8 mmol). The reaction mixture was stirred at ambient temperature for 2 hours and then at 86° C. (bath) for 2 hours. After cooling to ambient temperature, concentrated HCl (14.85 g, 407.3 mmol) and ether (200 mL) were added. The aqueous layer was separated and basified by K2CO3 (46.91 g, 339.4 mmol). To the resulting solution was added THF (150 mL) and Boc2O (37.04 g, 169.7 mmol). The reaction mixture was stirred at ambient temperature for 1 hour. Ethyl acetate (100 mL) was added. The organic layer was separated, washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (3:1 hexane/ethyl acetate) on silica gel to give (S)-benzyl 3-(tert-butoxycarbonylamino)-3-methylpyrrolidine-1-carboxylate (42.30 g, 126.5 mmol, 93.2% yield) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889704B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-16b6a6cc7d384ba79e025a721ae94d5d |
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| Source note | uspto-grants-2014_11 |
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