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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284631Generated: October 27, 2026

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

https://huagongshe.com/reaction/1284631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
Reactant3-(4-Phenylpiperazin-1-yl)propan-1-amineHCID 261297—
Productmethyl N-[3-(4-phenyl-1-piperazinyl)propyl]dithiocarbamateHCID 12802957—

Reaction Steps

To a solution of potassium hydroxide (2.85 g) in methanol (25 ml) was added 3-(4-phenyl-1-piperazinyl)propylamine (11.1 g) and thereto was added carbon disulfide (3.85 g) under ice cooling over a period of 10 minutes. The resulting mixture was stirred for 3 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 (7.2 g) with stirring. The resulting mixture was stirred for 2 hours under ice-cooling and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and then evaporated to give methyl N-[3-(4-phenyl-1-piperazinyl)propyl]dithiocarbamate (12.9 g), mp 75° to 79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563524
Source datasetuspto-grants-1986_01
ORD IDord-e65b8f4cf2294823bf1f928155d2de47
Source noteuspto-grants-1986_01