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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704711Generated: October 31, 2026

Thiophene → ethyl 4-aminohexahydro-1H-azepine-1-carboxylate

https://huagongshe.com/reaction/704711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
Reactantethyl hexahydro-4-[(phenylmethyl)amino]-1H-azepine-1-carboxylateHCID 15037322—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Productethyl 4-aminohexahydro-1H-azepine-1-carboxylateHCID 15037323100%

Reaction Steps

69.1 Parts of ethyl hexahydro-4-[(phenylmethyl)amino]-1H-azepine-1-carboxylate were hydrogenated in the prescence of a solution of thiophene in methanol 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 46.9 parts (100%) of ethyl 4-aminohexahydro-1H-azepine-1-carboxylate as a residue (interm. 28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988689
Source datasetuspto-grants-1991_01
ORD IDord-8ca89a50e4f54cea871e9d84da9ba004
Source noteuspto-grants-1991_01