HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460190Generated: October 25, 2026
Dicyclohexylcarbodiimide → Methyl 4-(2,3,4-trimethoxyphenylacetyl)-1-piperazinecarbodithioate
https://huagongshe.com/reaction/1460190
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2,3,4-Trimethoxyphenylacetic acid | HCID 89727 | — |
| Reactant | Methyl piperazine-1-carbodithioate | HCID 21278808 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(2,3,4-trimethoxyphenylacetyl)-1-piperazinecarbodithioate | HCID 19388512 | 48.8% |
Reaction Steps
In 6.2 ml of methylene chloride were dissolved 310 mg (1.37 mmol.) of 2,3,4-trimethoxyphenylacetic acid and 289 mg (1.64 mmol.) of methyl 1-piperazinecarbodithioate. To the solution was added 395 mg (1.92 mmol.) of dicyclohexylcarbodiimide. The mixture was stirred at room temperature for 1 hour. A precipitated solid was removed by filtration, and to the filtrate were added methylene chloride and 1-N hydrochloric acid. The organic solvent portion was taken out, washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and placed under reduced pressure to distill off the solvent. The residue was purified over a silica gel column. The obtained oil was crystallized from a mixture of ethanol and hexane, yielding 257 mg of the desired compound as a white crystalline product, m.p. 119°-120° C., yield 48.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05070089 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-a46d335b64cc465aa82a48abd19e2846 |
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| Source note | uspto-grants-1991_12 |
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