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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926534Generated: October 30, 2026

tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 118005515, compound

https://huagongshe.com/reaction/926534

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
Reactant5-Bromo-2-(trifluoromethyl)pyridineHCID 2761197—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118005515HCID 118005515—

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of isopropylmagnesium chloride (2.0 M in THF, 40.3 mL, 80.6 mmol) was added dropwise by syringe to a solution of 5-bromo-2-(trifluoromethyl)pyridine (19.5 g, 86.3 mmol) in dry THF (12 mL) at 2° C. After 30 minutes, tert-butyl 4-formylpiperidine-1-carboxylate (12.3 g, 57.3 mmol) was added to the Grignard solution at 2° C. as a solid. The reaction mixture was warmed to 10° C. over 1.5 hours after which it was quenched with saturated aqueous ammonium chloride solution. The mixture was partitioned between water and ethyl acetate. The separated aqueous phase was further extracted with ethyl acetate and washed with saturated aqueous NaCl solution. The organic phase was dried (MgSO4), filtered, and concentrated to afford the title compound which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-83e79849758643639a42a2fa306897bf
Source noteuspto-grants-2016_03