HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757563Generated: October 27, 2026
Sodium Carbonate → Methyl 4-(3-methoxybenzyl)-1-piperazinecarbodithioate
https://huagongshe.com/reaction/1757563
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Methoxybenzyl chloride | HCID 69994 | — |
| Reactant | Methyl piperazine-1-carbodithioate | HCID 21278808 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 4-(3-methoxybenzyl)-1-piperazinecarbodithioate | HCID 19388481 | 82.8% |
Reaction Steps
In a nitrogen atmosphere, 1.57 g (10.0 mmol.) of 3-methoxybenzyl chloride, 2.00 g (10.0 mmol., purity 88.1% of methyl 1-piperazinecarbodithioate, 1.06 g (10.0 mmol.) of anhydrous sodium carbonate and 20 ml of ethanol. The mixtrue was refluxed under heating for 5 hours. The solvent was distilled off under reduced pressure. The residue was mixed with 15 ml of dichloromethane and 10 ml of water. The mixture was allowed to give separated layers. The organic solvent portion was washed with water and a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and placed under reduced pressure to distill off the solvent. Theresidue was purified over a silica gel column to give 2.46 g of methyl 4-(3-methoxybenzyl)-1-piperazinecarbodithioate as a colorless crystalline product, yield 82.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05446146 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-ef57e3f420914cf7aec4f0854115f611 |
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| Source note | uspto-grants-1995_08 |
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