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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283750Generated: October 26, 2026

Ethyl chloroformate → 2-Ethoxycarbonyloxyimino-2-cyanoacetic acid amide

https://huagongshe.com/reaction/1283750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantSodium BicarbonateHCID 516892—
ReactantSodiumHCID 5360545—
Reactant2-Cyano-2-hydroxyiminoacetamideHCID 6762443—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-Ethoxycarbonyloxyimino-2-cyanoacetic acid amideHCID 5456565087.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of water (100 ml) and acetone (15 ml), sodium salt of 2-hydroxyimino-2-cyanoacetic acid amide (19.6 g) is added, and the obtained solution in which a part of the sodium salt is present in a suspended state is cooled at 0°C. Ethyl chloroformate (15 g) is dropwise added thereto, and the resulting mixture is, after adjusted to pH 7 to 8 with the addition of an aqueous solution of sodium hydrogencarbonate, stirred at room temperature for 1 hour and then filtered to collect the precipitated crystals. To the filtrate, a small amount of acetonitrile is added, and the mixture is extracted with ether. The ether layer is washed with water, dried and concentrated to give crystals, which are put together with the above obtained crystals to obtain 2-ethoxycarbonyloxyimino-2-cyanoacetic acid amide (22.5 g). A part of the product is recrystallized from ethyl acetate to give crystals melting at 194° to 196°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03976635
Source datasetuspto-grants-1976_08
ORD IDord-4f713c75f9c94f4fabe9e975c9ba1d94
Source noteuspto-grants-1976_08