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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934406Generated: November 1, 2026

Ethyl cyanoacetate → 2-Cyano-4-oxohexanoic acid ethyl ester

https://huagongshe.com/reaction/1934406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
Reactant1-Bromo-2-butanoneHCID 13156—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventBenzeneHCID 241—
Product2-Cyano-4-oxohexanoic acid ethyl esterHCID 5367539988.9%

Reaction Steps

To a 5° C. solution containing 27.8 g (246 mmol) of ethyl cyanoacetate and 38.2 g (251 mmol) of 1,8-diazabicyclo[5.4.0]undec-7ene in 420 mL of benzene was added over 30 minutes a solution of 1-bromo-2-butanone in 70 mL of benzene. The ice bath was removed and the reaction stirred for 1 hour at ambient temperature. At this time, the solids were removed by filtration and washed with 100 mL of methyl tert-butyl ether. The filtrate and the wash were combined and concentrated. The crude product was purified by short path distillation (0.2 torr, 140° C.) to provide 40.0 g (88.9%) of 2-cyano-4-oxohexanoic acid ethyl ester as a colorless oil. nmr (500 MHz, CDCl3) δ1.09 (t, J=7.3 Hz, 3H), 1.31 (t, J=7.1 Hz, 3H), 2.50 (q, J=7.3 Hz, 2H), 2.96 (dd, J=5.5, 18.0 Hz, 1H), 3.16 (dd, J=7.2, 18.0 Hz, 1H), 3.96 (dd, J=5.5, 7.2 Hz, 1H), 4.25 (q, J=7.1 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384041B1
Source datasetuspto-grants-2002_05
ORD IDord-676790cff40a41eb9fc74883745c8bec
Source noteuspto-grants-2002_05