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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966148Generated: October 30, 2026

Diethyl (cyanomethyl)phosphonate → 3-(Cyanomethylene)-1-(methoxymethyl)cyclobutanecarbonitrile

https://huagongshe.com/reaction/1966148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-(Methoxymethyl)-3-oxocyclobutane-1-carbonitrileHCID 66824330—
SolventTetrahydrofuranHCID 8028—
Product3-(Cyanomethylene)-1-(methoxymethyl)cyclobutanecarbonitrileHCID 66824512—

Reaction Steps

To a solution of 1.0000 M of potassium tert-butoxide in tetrahydrofuran (2.25 mL) at 0° C. was added dropwise a solution of diethyl cyanomethylphosphonate (0.381 mL, 0.00236 mol) in tetrahydrofuran (4 mL, 0.05 mol). The reaction was warmed to rt and then cooled to 0° C. again. To the reaction mixture was added a solution of 1-(methoxymethyl)-3-oxocyclobutanecarbonitrile (0.298 g, 0.00214 mol) in tetrahydrofuran (2 mL, 0.02 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 used directly in next step. LCMS calculated for C9H11N2O(M+H)+: 163.1. Found: 163.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420629B2
Source datasetuspto-grants-2013_04
ORD IDord-27f688aa7bf54ad28d3e367115842a69
Source noteuspto-grants-2013_04