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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226396Generated: October 30, 2026

Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → HCID 86603705, compound

https://huagongshe.com/reaction/226396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
ReactantHCID 86603706HCID 86603706—
CatalystHCID 178418406HCID 178418406—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86603705HCID 8660370589.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of tert-butyl (3R)-3-{[5-(hydroxymethyl)-2-pyridinyl]amino}-1-piperidinecarboxylate (3.65 g, 11.9 mmol) in dioxane (50 mL) was added manganese(IV) oxide (7.7 g, 89 mmol) and (carbethoxymethylene)triphenylphosphorane (6.2 g, 17.8 mmol). After stirring for 18 hrs at 60° C., a resulting precipitate was filtered and the filtrate was evaporated in vacuo and the residue was partitioned between water and EtOAc. The organic layer was separated, washed water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography (CHCl3/methanol=95/5)to give tert-butyl (3R)-3-({5-[(1E)-3-ethoxy-3-oxo-1-propen-1-yl]-2-pyridinyl}amino)-1-piperidinecarboxylate (3.99 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-9af851f3e68942a2a0a52be966159663
Source noteuspto-grants-2009_07