HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325906Generated: October 25, 2026
Methanol → methyl N-[3-(4-phenyl-1-piperazinyl)propyl]dithiocarbamate
https://huagongshe.com/reaction/325906
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(4-Phenylpiperazin-1-yl)propan-1-amine | HCID 261297 | — |
| Product | methyl N-[3-(4-phenyl-1-piperazinyl)propyl]dithiocarbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04443443 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-47a37082f86147eb8754f6b794732fcd |
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| Source note | uspto-grants-1984_04 |
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