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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718241Generated: October 29, 2026

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

https://huagongshe.com/reaction/718241

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 numberUS09193741B2
Source datasetuspto-grants-2015_11
ORD IDord-a1eec9e787364fe78fb1c5e909beb2e2
Source noteuspto-grants-2015_11