HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412584Generated: October 29, 2026
Water → Tert-butyl 4-cyano-4-(2-hydroxyethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/412584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | 4-Cyano-4-(2,3-dihydroxypropyl)piperidine-1-carboxylic acid tert-butyl ester | HCID 60064175 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-cyano-4-(2-hydroxyethyl)piperidine-1-carboxylate | HCID 60064207 | 95.9% |
Reaction Steps
To a solution of 4-cyano-4-(2,3-dihydroxypropyl)piperidine-1-carboxylic acid tert-butyl ester (3.65 g) in tetrahydrofuran (100 ml) was added 10% aqueous sodium periodate solution (100 ml), and the mixture was stirred at room temperature for 40 min. After completion of the reaction, water was added and the mixture was extracted with ethyl acetate and washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated. The obtained residue (3.3 g) was dissolved in tetrahydrofuran (100 ml) and sodium borohydride (360 mg) and methanol (20 ml) were added with ice-cooling, and the mixture was stirred at room temperature for 30 min. After completion of the reaction, 10% aqueous citric acid was added and the mixture was extracted with ethyl acetate and washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated. The obtained residue was purified by silica gel column chromatography (chloroform:methanol=95:5) and dried under reduced pressure to give the title compound (3.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562828B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-76f457d9a39741b0bf617669a7e6329d |
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| Source note | uspto-grants-2003_05 |
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