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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879643Generated: October 29, 2026

Tert-butyl 4-hydroxypiperidine-1-carboxylate → HCID 49759211, compound

https://huagongshe.com/reaction/1879643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
Reactant5-Fluoro-2-nitroanisoleHCID 2779250—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 49759211HCID 4975921143.6%

Reaction Steps

To a mixture of tert-butyl 4-hydroxypiperidine-1-carboxylate (1.49 g) and tetrahydrofuran (30 mL), potassium tert-butoxide (830 mg) was added under ice cooling and stirred for 30 minutes, followed by addition of a mixture of 4-fluoro-2-methoxy-1-nitrobenzene (1.00 g) and tetrahydrofuran (20 mL). After stirring at room temperature for 3 hours, the reaction mixture was extracted by addition of water and ethyl acetate, washed with saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; n-hexane:diethyl ether=4:1) to give tert-butyl 4-(3-methoxy-4-nitrophenoxy)piperidine-1-carboxylate (898 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318702B2
Source datasetuspto-grants-2012_11
ORD IDord-81bd906ac1ce4334a3d0cb42c221f60c
Source noteuspto-grants-2012_11