Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346532Generated: October 30, 2026

Ethyl formate → Sodium (E)-2-cyano-2-[(methoxycarbonyl)(methyl)amino]ethenolate

https://huagongshe.com/reaction/346532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl cyanomethyl(methyl)carbamateHCID 45087346—
SolventTetrahydrofuranHCID 8028—
ProductSodium (E)-2-cyano-2-[(methoxycarbonyl)(methyl)amino]ethenolateHCID 57469797—

Reaction Steps

0.46 g (0.01 mmol) of sodium methoxide is added under argon to tetrahydrofuran (solution A). Then 1.00 g (0.01 mmol) of methyl cyanomethyl(methyl)carbamate from Example 9A is added to 1.73 g (0.02 mmol) of ethyl formate. Solution A is slowly added dropwise to this mixture. The mixture is stirred at RT overnight. The solvent is concentrated in vacuo in a rotary evaporator, and diethyl ether is added to the residue. The crystals which have separated out are filtered off with suction and dried under high vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173037B2
Source datasetuspto-grants-2007_02
ORD IDord-78a196e817e64eb8ab1ec95dfae2af59
Source noteuspto-grants-2007_02