HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325903Generated: October 26, 2026
Methanol → methyl N-[3-(4-isopropyl-1-piperazinyl)propyl]dithiocarbamate
https://huagongshe.com/reaction/325903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(4-Isopropyl-piperazin-1-yl)-propylamine | HCID 12802956 | — |
| Product | methyl N-[3-(4-isopropyl-1-piperazinyl)propyl]dithiocarbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04443443 |
|---|
| Source dataset | uspto-grants-1984_04 |
|---|
| ORD ID | ord-d728dec553b2404cbd7da5dceadcdd54 |
|---|
| Source note | uspto-grants-1984_04 |
|---|