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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501889Generated: November 1, 2026

Water → HCID 12148215, compound

https://huagongshe.com/reaction/1501889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178418507HCID 178418507—
SolventDichloromethaneHCID 6344—
ProductHCID 12148215HCID 12148215—

Reaction Steps

To a solution of tert-butyl 4-oxopiperidine-1-carboxylate (1.00 g, 5.02 mmol) in 20 mL of dichloromethane at 0° C. under an atmosphere of nitrogen was added vinylmagnesium bromide (0.7 M dichloromethane solution, 9.32 mL, 6.52 mmol) dropwise. After 1 hr, the mixture was treated with water and extracted 3× with ethyl acetate. The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified via silica gel chromatography, eluting with 0-60% ethyl acetate in hexanes, to provide tert-butyl 4-ethenyl-4-hydroxypiperidine-1-carboxylate that gave a proton NMR spectra consistent with theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206200B2
Source datasetuspto-grants-2015_12
ORD IDord-d7ce98ae62bc4eae9fbeabbc3cd5a20f
Source noteuspto-grants-2015_12