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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341334Generated: October 27, 2026

Ethyl cyanoacetate → HCID 71530805, compound

https://huagongshe.com/reaction/341334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantAmmonium ChlorideHCID 25517—
Reactant(Iodomethyl)trimethylsilaneHCID 77877—
ReactantSodium ethoxideHCID 2723922—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 71530805HCID 7153080583.5%

Reaction Steps

A solution of ethyl cyanoacetate (5.34 g, 47.3 mmol) in dimethyl sulfoxide (DMSO, 20 ml) was added portionwise with sodium ethoxide (3.21 g, 47.2 mmol), and the mixture was stirred at room temperature for 4 hours with occasionally cooling the mixture on ice when temperature elevation was observed. The reaction mixture was put on an ice bath, and added dropwise with a solution of iodomethyltrimethylsilane (7.78 g, 36.4 mmol) in DMSO (5 ml), and the mixture was stirred at room temperature for 24 hours. The reaction mixture was added with saturated aqueous ammonium chloride, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by silica gel chromatography [hexane/ethyl acetate (49:1)] to obtain ethyl 3-(trimethylsilyl)-2-cyanopropionate (6.06 g, 65%) mentioned in the title as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895769B2
Source datasetuspto-grants-2014_11
ORD IDord-98ad2bde8c044412b36dde6be0e975e6
Source noteuspto-grants-2014_11