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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966145Generated: October 30, 2026

Diethyl (cyanomethyl)phosphonate → HCID 66824457, compound

https://huagongshe.com/reaction/1966145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-methyl-3-oxocyclobutane-1-carbonitrileHCID 66824709—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66824457HCID 6682445746.84%

Reaction Steps

To a solution of 1.0 M of potassium tert-butoxide in tetrahydrofuran (52.9 mL) at 0° C. was added dropwise a solution of diethyl cyanomethylphosphonate (8.98 mL, 0.0555 mol) in tetrahydrofuran (90 mL, 1 mol). The reaction was warmed to rt and then cooled at 0° C. again. To the reaction mixture was added a solution of 1-methyl-3-oxocyclobutanecarbonitrile (5.50 g, 0.0504 mol) in tetrahydrofuran (40 mL, 0.6 mol). The reaction was allowed to warm up to rt and stirred at rt overnight. After quenching with water, the mixture was extracted with ether. The combined organic layers were washed with water, brine, dried and evaporated to dryness. The crude mixture was purified on silica gel, eluting with 0 to 60% EtOAc in hexane, to give the desired product (3.12 g, 46.84%). LCMS calculated for C8H9N2(M+H)+: 133.1. Found: 133.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420629B2
Source datasetuspto-grants-2013_04
ORD IDord-ea6ee2004c4848d7bca0f79f19295584
Source noteuspto-grants-2013_04