HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538452Generated: October 26, 2026
Isopropanol → Tert-butyl 4-(4-cyanobenzyl)-4-hydroxypiperidine-1-carboxylate
https://huagongshe.com/reaction/538452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Tert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylate | HCID 70851437 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(4-cyanobenzyl)-4-hydroxypiperidine-1-carboxylate | HCID 70851493 | — |
Reaction Steps
A mixture of tert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylate (35 g), K4Fe(CN)6 (12 g), palladium(II) acetate (1.1 g), sodium carbonate (11 g), 2-propanol (7.5 mL) and DMA (150 mL) was stirred at 120° C. for 12 hr. The reaction mixture was allowed to cool to room temperature, diluted with dichloromethane, and filtered through celite. The filtrate was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (17 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865717B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-2b67cd4fd48b46779c75e1abd811e127 |
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| Source note | uspto-grants-2014_10 |
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