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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284628Generated: October 25, 2026

Methanol → methyl N-[3-(4-isopropyl-1-piperazinyl)propyl]dithiocarbamate

https://huagongshe.com/reaction/1284628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
Reactant3-(4-Isopropyl-piperazin-1-yl)-propylamineHCID 12802956—
Productmethyl N-[3-(4-isopropyl-1-piperazinyl)propyl]dithiocarbamateHCID 20252225—

Reaction Steps

To a solution of potassium hydroxide (4.9 g) in methanol (40 ml) was added 3-(4-isopropyl-1-piperazinyl)propylamine (14.7 g) and thereto was added carbon disulfide (6.0 g) under ice cooling over a period of 20 minutes. The resulting mixture was stirred for 3.5 hours under ice cooling. The reaction mixture was evaporated under reduced pressure. The residual oil was dissolved in water (40 ml) and washed with diethyl ether. The washed aqueous layer was ice-cooled and thereto was added methyl iodide (11.3 g) with stirring over a period of about 5 minutes. The resulting mixture was stirred for 2 hours under ice-cooling extracted with chloroform. The extract was washed with water, dried over magnesium sulfate and then evaporated to give an oil of methyl N-[3-(4-isopropyl-1-piperazinyl)propyl]dithiocarbamate (15.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563524
Source datasetuspto-grants-1986_01
ORD IDord-ee313229b9e143e381a7ccb5a9d71667
Source noteuspto-grants-1986_01