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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643548Generated: October 29, 2026

Triethylamine → HCID 57880560, compound

https://huagongshe.com/reaction/643548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
SolventDimethylformamideHCID 6228—
ProductHCID 57880560HCID 57880560—

Reaction Conditions

Temperature0 °C

Reaction Steps

A cooled (0° C.) solution of Boc-isonipecotic acid (5.97 g, 26.0 mmol) and Meldrum's acid (3.75 g, 26.0 mmol) in DMF (54 mL) was treated dropwise with diethyl cyanophosphonate (4.34 mL, 28.6 mmol) and triethylamine (11.2 mL, 80.7 mmol). After stirring at 0° C. for an additional 30 min the reaction mixture was permitted to warm to rt and stir over 3 days. The reaction mixture was concentrated under reduced pressure and ether and 1N HCl solution were added. The aqueous layer was extracted again with ether and the ethereal layers were combined and washed with 1N HCl solution, twice with water, and lastly with brine. He ethereal layer was then dried over anhydrous MgSO4, filtered, and concentrated to give tert-butyl 4-[(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)(hydroxy)methyl]piperidine-1-carboxylate which contained approximately 10% of Boc-isonipecotic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700591B2
Source datasetuspto-grants-2010_04
ORD IDord-ae79c3c7c95542cd9d420ddc0e26cb8e
Source noteuspto-grants-2010_04