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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966141Generated: October 30, 2026

Water → Ethyl 3-(cyanomethylene)cyclobutanecarboxylate

https://huagongshe.com/reaction/1966141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
ReactantEthyl 3-oxocyclobutanecarboxylateHCID 22467070—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(cyanomethylene)cyclobutanecarboxylateHCID 57868872—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium hydride (60% dispersion in mineral oil, 0.730 g, 18.3 mmol) in tetrahydrofuran (100 mL) at 0° C. was added diethyl cyanomethylphosphonate (3.22 mL, 19.9 mmol), dropwise. The cooling bath was removed and the reaction was allowed to reach room temperature and was stirred at this temperature for 45 minutes. The solution was re-cooled to 0° C. and a solution of ethyl 3-oxocyclobutanecarboxylate (2.36 g, 16.6 mmol) in tetrahydrofuran (50 mL) was introduced dropwise. After stirring for 2 hours, water and ethyl ether were added into the reaction. The layers were separated and the aqueous portion extracted with two further portions of ether. The combined extracts were washed with brine, dried over sodium sulfate, decanted and concentrated. The residue was azeotroped once with toluene to afford product, used without further purification in Step 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420629B2
Source datasetuspto-grants-2013_04
ORD IDord-b878d762a80f49408dd8c3a8e21efbd1
Source noteuspto-grants-2013_04