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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396709Generated: October 31, 2026

Trimethylsilyl iodide → N-(3-Methylphenyl)piperazine-1-carboxamide

https://huagongshe.com/reaction/1396709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 2986625HCID 2986625—
SolventDichloromethaneHCID 6344—
ProductN-(3-Methylphenyl)piperazine-1-carboxamideHCID 16769291100%

Reaction Steps

A suspension of ethyl 4-(m-tolylcarbamoyl)piperazine-1-carboxylate (example 59, 1.5 g, 5.15 mmol) in dichloromethane (25 ml) was treated dropwise at room temperature with iodotrimethylsilane (1.6 ml, 11.3 mmol). The reaction mixture was stirred under nitrogen at room temperature overnight. The volatiles were evaporated to dryness, diluted with methanol and the solid was filtered off. The solid was washed with methanol and dichloromethane and dried under vacuum to yield the title compound as a yellow solid (1.1 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901132B2
Source datasetuspto-grants-2014_12
ORD IDord-e1b90950d32c406783a749133af69b4b
Source noteuspto-grants-2014_12