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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408634Generated: October 29, 2026

Ethyl bromoacetate → Diethyl 3-cyano-3-(6-methoxypyridin-3-yl)pentanedioate

https://huagongshe.com/reaction/408634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
Reactant(6-Methoxypyridin-3-yl)acetonitrileHCID 45079846—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 3-cyano-3-(6-methoxypyridin-3-yl)pentanedioateHCID 67493644—

Reaction Conditions

Temperature-78 °C

Reaction Steps

10.12 ml (20.25 mmol) of lithium diisopropylamide are introduced in 22 ml of anhydrous tetrahydrofuran in a 100 ml three-necked round-bottomed flask under an argon atmosphere at −78° C. 1.00 g (6.75 mmol) of (6-methoxypyridin-3-yl)acetonitrile (WO2004/111031) in solution of 5 ml of anhydrous tetrahydrofuran is added. The reaction mixture is subsequently brought back gently to 0° C. and stirred at this temperature for one hour. The reaction medium is then cooled to −78° C. and 2.25 ml (20.25 mmol) of ethyl bromoacetate are added dropwise. The resulting mixture is subsequently brought back slowly to ambient temperature and then left stirring for 12 hours. The reaction medium is subsequently poured into a saturated aqueous ammonium chloride solution and extracted twice with diethyl ether. The organic phases are combined, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue obtained is purified by chromatography on a column of silica gel, elution being carried out with a mixture of cyclohexane and ethyl acetate in the proportions of 90/10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759343B2
Source datasetuspto-grants-2014_06
ORD IDord-11c1c274c0eb498fa6646de13cb33a59
Source noteuspto-grants-2014_06