HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386814Generated: November 2, 2026
tert-Butyl 4-formylpiperidine-1-carboxylate → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1386814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 2764081 | 89% |
Reaction Steps
To a solution of 0.434 g of 4-formyl-piperidine-1-carboxylic acid, tert-butyl ester (from Step A) in 15 ml THF was added sodium borohydrid at 0° C. and stirred at 0° C. for 20 mn. The reaction was warmed to rt and stirred at rt for 14 hours. After quenching with CH3OH, the reaction mixture was concentrated, then partitioned between EtOAc and H2O. The aqueous layer was extracted with 2×20 mL of EtOAc. The combined organic phases were washed with brine, dried over MgSO4 and concentrated. The residue was purified by flash chromatography eluting with 50% EtOAc in hexane, then 100% EtOA to give 390 mg of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265434B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-9efc596fe4114e43b9f6c3b8657e0635 |
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| Source note | uspto-grants-2001_07 |
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