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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443215Generated: October 30, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → N-t-Butoxycarbonyl-4-(3-methylphenyl)-4-hydroxy piperidine

https://huagongshe.com/reaction/443215

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178425413HCID 178425413—
SolventTetrahydrofuranHCID 8028—
ProductN-t-Butoxycarbonyl-4-(3-methylphenyl)-4-hydroxy piperidineHCID 21193300—

Reaction Steps

To a solution of 3-methylphenyl magnesium bromide (58 ml of a 1M solution in THF, 58.0 mmol) at 0° C. was added a solution of N-t-butoxycarbonyl piperidin-4-one (10.0 g, 53mmol) in THF (30 ml) dropwise over 20 min, and the reaction stirred under argon for a further 30 min. The reaction was quenched by addition of sat NH4Cl solution (100 ml), and diluted with EtOAc. The organic extracts were dried, (MgSO4) and the solvent evaporated in vacuo to afford the title compound of sufficient purity to be used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-199e1ccf53034887a75bfc106a82106f
Source noteuspto-grants-1999_04