Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570513Generated: October 28, 2026

Malononitrile → Methyl 3,3-dicyano-2,2-dimethylpropanoate

https://huagongshe.com/reaction/570513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalononitrileHCID 8010—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-bromo-2-methylpropionateHCID 90097—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3,3-dicyano-2,2-dimethylpropanoateHCID 86657403—

Reaction Steps

In THF (91 ml), 1.816 g (45.411 mmol) of sodium hydride (60% in mineral oil) were admixed gradually with 3 g (45.411 mmol) of malononitrile. Subsequently, 5.876 ml (45.411 mmol) of methyl 2-bromo-2-methylpropanoate were added and the reaction mixture was stirred at room temperature overnight. Thereafter, another 5.876 ml (45.411 mmol) of methyl 2-bromo-2-methylpropanoate were added and the reaction mixture was heated to 50° C. overnight. Then yet another 1.762 ml (13.623 mmol) of methyl 2-bromo-2-methylpropanoate were added and the reaction mixture was heated to 50° C. for a further 4 h. The mixture was then admixed with saturated aqueous sodium hydrogencarbonate solution and extracted three times with ethyl acetate. The combined organic phases were washed with saturated aqueous sodium chloride solution, dried over sodium sulphate, filtered and concentrated to dryness. This gave 8.9 g of crude product, which was purified by chromatography on silica gel (4:1 cyclohexane-ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023849B2
Source datasetuspto-grants-2015_05
ORD IDord-afe7f3ee07c546c69e57f1b6096650e2
Source noteuspto-grants-2015_05