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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886393Generated: October 31, 2026

Ethyl cyanoacetate → HCID 15037319, compound

https://huagongshe.com/reaction/1886393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantThiopheneHCID 8030—
ReactantTriethylamineHCID 8471—
ReactantHCID 68866648HCID 68866648—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 15037319HCID 1503731999.8%

Reaction Steps

A mixture of 56 parts of ethyl hexahydro-4-oxo-1H-azepinecarboxylate, 40 parts of ethyl 2-cyanoacetate, 60 parts of N,N-diethylethanamine, 400 parts of methanol and 3 parts of thiophene in methanol 4% was hydrogenated at normal pressure and at room temperature with 4 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated, yielding 84.6 parts (99.8%) of ethyl α-cyano-1-(ethoxycarbonyl)hexahydro-1H-azepine-4-acetate as a residue (int. 24).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151424
Source datasetuspto-grants-1992_09
ORD IDord-c125e561350d493aa8fab9d316bf0c32
Source noteuspto-grants-1992_09