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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876853Generated: November 2, 2026

Diethyl (cyanomethyl)phosphonate → HCID 67054937, compound

https://huagongshe.com/reaction/1876853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67054937HCID 6705493793.8%

Reaction Steps

To a solution of 1.0 M of potassium tert-butoxide in tetrahydrofuran (24.6 mL) at 0° C. was added dropwise a solution of diethyl cyanomethylphosphonate (4.18 mL, 0.0258 mol) in tetrahydrofuran (31.40 mL). The reaction was warmed to room temperature and then cooled to 0° C. again. To the reaction mixture was added a solution of tert-butyl 4-formylpiperidine-1-carboxylate (5.0 g, 0.023 mol) in tetrahydrofuran (6.28 mL). The reaction was allowed to warm up to room temperature and stirred at room temperature overnight. After being quenched with water, the mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried and evaporated to dryness. The crude mixture was purified on silica gel, eluting with 0 to 50% EtOAc in hexanes, to give the desired product (5.10 g, 92%). LCMS (M+Na) 259.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309718B2
Source datasetuspto-grants-2012_11
ORD IDord-3c833196f83e4f638b988d661512e67c
Source noteuspto-grants-2012_11