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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281479Generated: November 1, 2026

N-Methyl-4-nitroaniline → N-methyl-N-(4-nitrophenyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/2281479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-4-nitroanilineHCID 7483—
ReactantTriethylamineHCID 8471—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-methyl-N-(4-nitrophenyl)cyclopropanecarboxamideHCID 66878005—

Reaction Steps

To a mixture of N-methyl-4-nitroaniline (2 g, 13.1 mmol) in DCM (30 mL) was added Et3N (2.75 mL, 20 mmol) and cyclopropanecarbonyl chloride (1.32 mL, 14.4 mmol) at room temperature, after stirring for 1 h at room temperature, the mixture was diluted with EtOAc, the organics was washed with Sat. NaHCO3, brine, dried and concentrated to give N-methyl-N-(4-nitrophenyl)cyclopropanecarboxamide as crude product (3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139581B2
Source datasetuspto-grants-2015_09
ORD IDord-3384c6a337a04c569622d7d576e08ba6
Source noteuspto-grants-2015_09