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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978861Generated: October 27, 2026

Methyl cyanoacetate → Methyl 3-amino-3-phenylprop-2-enoate

https://huagongshe.com/reaction/1978861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl cyanoacetateHCID 7747—
ReactantBromobenzeneHCID 7961—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductMethyl 3-amino-3-phenylprop-2-enoateHCID 6692010673.4%

Reaction Steps

47 g of bromobenzene in 90 ml of ether were added dropwise to 7.2 g of magnesium in 20 ml of ether under reflux, and the stirred mixture was refluxed for 1 hour. Thereafter, 9.9 g of methyl cyanoacetate were added dropwise while cooling with ice, and stirring was carried out for 1 hour at room temperature, for 5 hours under reflux and again for 15 hours at room temperature. 300 ml of ammonium chloride were carefully added to the reaction mixture and the aqueous phase was extracted twice with ether and the combined organic phases were washed three times with water, dried over sodium sulfate and evaporated down. The residue was distilled under greatly reduced pressure. 13 g of methyl β-amino-cinnamate were obtained (110-112° C., 10.15 mbar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239074B1
Source datasetuspto-grants-2001_05
ORD IDord-ec469162d2da4e20908f7efe0dc16a10
Source noteuspto-grants-2001_05