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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69112Generated: October 29, 2026

4,7-Diphenyl-1,10-phenanthroline → Tert-butyl 4-[(vinyloxy)methyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/69112

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,7-Diphenyl-1,10-phenanthrolineHCID 72812—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
Catalystpalladium(II) acetateHCID 167845—
SolventButyl vinyl etherHCID 8108—
ProductTert-butyl 4-[(vinyloxy)methyl]piperidine-1-carboxylateHCID 866943169,182.5%

Reaction Steps

4.3 g of tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate, 66 mg of 4,7-diphenyl-1,10-phenanthroline, and 45 mg of palladium acetate were added to 50 mL of butylvinyl ether, followed by stirring at room temperature for 15 minutes, and stirring at 75° C. for 2 days. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain 4.4 g of tert-butyl 4-[(vinyloxy)methyl]piperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822448B2
Source datasetuspto-grants-2014_09
ORD IDord-2390eb3d0a4647d3b0b617a4197dcc83
Source noteuspto-grants-2014_09