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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400608Generated: October 29, 2026

Trifluoroacetic acid → tert-butyl (3R)-3-(aminooxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/2400608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl (3S)-3-[({[(2S,5R)-7-oxo-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]pyrrolidine-1-carboxylateHCID 86693917—
SolventDichloromethaneHCID 6344—
Producttert-butyl (3R)-3-(aminooxy)pyrrolidine-1-carboxylateHCID 8669391162.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of tert-butyl (3S)-3-[({[(2S,5R)-7-oxo-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]pyrrolidine-1-carboxylate 10 (0.11 g, 0.24 mmol) in DCM (4.0 mL) was added trifluoroacetic acid (0.20 mL) at 0° C. The mixture was stirred at 0° C. for 1 h, concentrated and washed with ether. The white solid was collected by centrifugation. The crude product was purified by preparative HPLC to provide Compound 2 (Table 1)(30.4 mg, 36%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796257B2
Source datasetuspto-grants-2014_08
ORD IDord-e32fc8f99a3247ed8c5d0a7c36bf50ca
Source noteuspto-grants-2014_08