Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 67232594 | HCID 67232594 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Thiosulfate | HCID 24477 | — |
| Product | HCID 44828616 | HCID 44828616 | 88% |
Reaction Steps
To a mixed solution of tert-butyl (3R,4S)-3-{[(4R)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]carbonyl}-4-(4-fluorophenyl)pyrrolidine-1-carboxylate (0.32 g) obtained in step 2 in THF (14.4 mL) and water (4.8 mL) were added 30% aqueous hydrogen peroxide (939 μL) and 4N aqueous lithium hydroxide solution (518 μL) at 0° C., and the mixture was stirred at room temperature for 8 hr. The reaction mixture was diluted with aqueous sodium thiosulfate solution, and extracted with ethyl acetate. The extract was washed with water and extracted with 0.5N aqueous sodium hydroxide solution. The extract was washed with ethyl acetate, acidified with 10% aqueous citric acid solution, and extracted with ethyl acetate. The extract was washed with water and saturated brine, dried and concentrated under reduced pressure to give (3R,4S)-1-(tert-butoxycarbonyl)-4-(4-fluorophenyl)pyrrolidine-3-carboxylic acid (0.185 g, 88%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592454B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-8246a21cc4f44264b919c0e74b0e4750 |
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| Source note | uspto-grants-2013_11 |
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