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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876880Generated: November 1, 2026

Diethyl (cyanomethyl)phosphonate → HCID 66824380, compound

https://huagongshe.com/reaction/1876880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
Reactant3-Oxocyclobutane-1-carbonitrileHCID 13082390—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66824380HCID 6682438023.3%

Reaction Steps

To a solution of 1.0 M of potassium tert-butoxide in tetrahydrofuran (78.4 mL) at 0° C. was added drop wise a solution of diethyl cyanomethylphosphonate (13.3 mL, 0.0822 mol) in tetrahydrofuran (100 mL, 2 mol). The reaction was warmed to room temperature and then cooled at 0° C. again. To the reaction mixture was a solution of 3-oxocyclobutanecarbonitrile (7.10 g, 0.0746 mol) in tetrahydrofuran (70 mL). The reaction was allowed to warm up to room temperature and stirred overnight. After being quenched with water, the mixture was extracted with ether. The combined organic layers were washed with water, brine, dried over MgSO4, and evaporated to dryness. The crude mixture was purified on silica gel, eluting with 0 to 40% EtOAc in hexanes, to give the desired product (2.05 g, 23.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309718B2
Source datasetuspto-grants-2012_11
ORD IDord-05e17778aef3428a9bc002871ea9cd72
Source noteuspto-grants-2012_11