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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 276408189%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-9efc596fe4114e43b9f6c3b8657e0635
Source noteuspto-grants-2001_07