HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533376Generated: October 27, 2026
3-Cyanopyridine → (S)-3-oxiranylpyrrolidine-1-carboxylic acid t-butyl ester
https://huagongshe.com/reaction/533376
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Cyanopyridine | HCID 79 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | (R)-tert-Butyl 3-vinylpyrrolidine-1-carboxylate | HCID 46222798 | — |
| Catalyst | HCID 178477782 | HCID 178477782 | — |
| Product | (S)-3-oxiranylpyrrolidine-1-carboxylic acid t-butyl ester | HCID 86650332 | 63.9% |
Reaction Steps
To (R)-3-vinylpyrrolidine-1-carboxylic acid t-butyl ester (6.1 g, 30.8 mmol) was added 3-pyridinecarbonitrile (320 mg, 3.1 mmol) and methyltrioxorhenium(VII) (192 mg, 769 μmol). The mixture was stirred until homogeneous. The mixture was placed in an ice water bath and 30% hydrogen peroxide (33:77, hydrogen peroxide:H2O, 4.08 mL, 40.0 mmol) was added, while keeping the temperature below 35° C. The mixture was stirred for 2 hours. Additional methyltrioxorhenium(VII) (50 mg) was added and the mixture was stirred for 2 hours. The organic layer was collected and washed with a saturated sodium metabisulfite solution (10 mL) under an ice bath. The material was then washed with saturated aqueous NaCl. The organic layer was collected, dried over Na2SO4, filtered, and concentrated. The crude product was purified by column chromatography (0-100% EtOAc in hexanes) to give (S)-3-oxiranylpyrrolidine-1-carboxylic acid t-butyl ester as a yellowish oil (4.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853255B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f974cbea63b348529ac8b21a02bcc5c9 |
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| Source note | uspto-grants-2014_10 |
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