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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856132Generated: October 30, 2026

Potassium Iodide → Tert-butyl[4-(2-methyl-2-oxiranylmethyl)piperazin-1-yl]carbamate

https://huagongshe.com/reaction/856132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantTriethylamineHCID 8471—
Reactant2-Methyloxiran-2-ylmethyl paratoluenesulfonateHCID 14237194—
Reactanttert-Butyl piperazin-1-ylcarbamateHCID 21701658—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductTert-butyl[4-(2-methyl-2-oxiranylmethyl)piperazin-1-yl]carbamateHCID 2308116451.3%

Reaction Steps

A mixture of (2-methyl-2-oxiranylmethyl) toluene-4-sufonate (9.75 g, 40.3 mmol), tert-butyl piperazin-1-yl-carbamate (6.75 g, 33.5 mmol) prepared in Reference Example 36, triethylamine (7 ml, 50.3 mmol) and potassium iodide (6.68 g, 33.5 mmol) in DMF (70 ml) was stirred at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The extract was washed with water and brine, dried over sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/acetone=4/1) to afford tert-butyl[4-(2-methyl-2-oxiranylmethyl)piperazin-1-yl]carbamate (4.66 g, yield 51%) as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-22d6755f544d4a72960a99d739fd7135
Source noteuspto-grants-2007_08