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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225950Generated: October 26, 2026

Ammonium Chloride → Ethyl 2-methylidenebutanoate

https://huagongshe.com/reaction/225950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Bromomethyl)acrylic acid ethyl esterHCID 310620—
ReactantHCID 178418546HCID 178418546—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-methylidenebutanoateHCID 291416—

Reaction Steps

To CuCN (26.9 g, dried in advance under vacuum) was added under nitrogen atmosphere about 500 ml of dry tetrahydrofuran. The mixture was kept at −78□, and 100 ml of methyl magnesium bromide (3.0M diethylether solution) was slowly added thereto under mechanical stirring. The thick mixture was stirred for about 30 minutes at −78□. Ethyl 2-bromomethylacrylate (28.9 g, 150 mmol, Synthetic method: Villieras, J. and Rambaud, M. Synthesis, 1982, 914) dissolved in about 30 ml of dry tetrahydrofuran was slowly added thereto. The temperature of the reaction mixture was slowly raised to room temperature over two hours. The reaction was completed by slowly adding saturated ammonium chloride solution (˜50 ml). The reaction mixture was filtered through Celite to remove the precipitates, and then washed with diethylether. The organic layer was washed with water and saturated sodium bicarbonate solution (300 ml×2), dried (anhydrous Na2SO4), and concentrated under reduced pressure to give 26.7 g (stoichiometric yield) of a transparent liquid. This liquid was identified by 1H-NMR (500 MHz, CDCl3) and was confirmed to be the title compound having about 75% of w/w purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557133B2
Source datasetuspto-grants-2009_07
ORD IDord-0734a27040d04436b3d796d9a2f36dc6
Source noteuspto-grants-2009_07