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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065827Generated: October 25, 2026

trans-N-Octyl-2-(4-nitrophenyl)cyclopropanecarboxamide → trans-N-octyl-2-(4-aminophenyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/1065827

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans-N-Octyl-2-(4-nitrophenyl)cyclopropanecarboxamideHCID 12854633—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Producttrans-N-octyl-2-(4-aminophenyl)cyclopropanecarboxamideHCID 12854635—

Reaction Steps

To a stirred solution of 6.2 g. of trans-N-octyl-2-(4-nitrophenyl)cyclopropanecarboxamide in 70 ml. of glacial acetic acid, at 85° C., was added 5.3 g. of iron powder, portionwise, during 10 minutes. The temperature was kept between 85° and 90° C. during the addition. At the end of the addition, stirring was continued at 85°-90° C. for 10 minutes, and then the hot reaction mixture was filtered. The filtrate was evaporated in vacuo, and the residue thus obtained was partitioned between 350 ml. of ethyl acetate and 150 ml. of saturated sodium chloride solution. The ethyl acetate layer was removed, dried using sodium sulfate, and evaporated in vacuo. This gave 5.4 g. of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04331683
Source datasetuspto-grants-1982_05
ORD IDord-2094a272cb414ea3839746e0bbc318a5
Source noteuspto-grants-1982_05