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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403503Generated: October 31, 2026

Tetrahydrofuran → HCID 12148215, compound

https://huagongshe.com/reaction/403503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178418507HCID 178418507—
SolventDiethyl EtherHCID 3283—
ProductHCID 12148215HCID 12148215—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Oxo-piperidine-1-carboxylic acid tert-butyl ester (2.5 g, 12.5 mmol) was dissolved in 25 ml of diethylether and cooled to 0° C. A 1M solution of vinylmagnesiumbromide in THF (16.3 ml, 16.31 mmol) was added dropwise at 0° C. After 90 min stirring at 0° C., the reaction mixture was quenched with NH4Cl solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2 SO4 and evaporated. The crude product was further purified by flash chromatography (silicagel, cyclohexane/ethylacetate 4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748435B2
Source datasetuspto-grants-2014_06
ORD IDord-46b1e50322bf4762a9dc53acefa69a13
Source noteuspto-grants-2014_06