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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338828Generated: October 25, 2026

Hydrochloric Acid → HCID 51041670, compound

https://huagongshe.com/reaction/338828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantBis(trifluoroacetoxy)iodobenzeneHCID 102317—
ReactantAcetonitrile--water (1/1)HCID 18373917—
Reactant(S)-benzyl 3-carbamoyl-3-methylpyrrolidine-1-carboxylateHCID 86707398—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 51041670HCID 5104167093.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-16b6a6cc7d384ba79e025a721ae94d5d
Source noteuspto-grants-2014_11