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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66817Generated: October 25, 2026

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

https://huagongshe.com/reaction/66817

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 numberUS04343813
Source datasetuspto-grants-1982_08
ORD IDord-7113f04168fd4797a9a04d003de2b0fb
Source noteuspto-grants-1982_08