HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 178509163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Dimethyl N-cyanodithioiminocarbonate | HCID 66289 | — |
| Reactant | 1-(2-Phenoxyethyl)piperazine | HCID 233187 | — |
| Product | HCID 178509163 | HCID 178509163 | — |
Reaction Steps
In the manner of Example 3 a mixture of 10.3 g (0.05 moles) of 1-[2-phenoxyethyl]piperazine and 7.3 g (0.05 moles) of dimethyl cyanodithioiminocarbonate in 250 ml of acetonitrile was refluxed for 3 hours. After cooling, 2.8 ml (0.056 moles) of hydrazine hydrate was added and the mixture was refluxed for 45 minutes. The mixture was cooled, filtered through diatomaceous earth and the filtrate was evaporated to a paste. The product was crystallized from ethanol/ether/hexane, collected and washed with ether and gave 5.3 g of colorless crystals, mp 131°-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04582833 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-0c592fc6242142c6a9a2d3228d1b756a |
| Source note | uspto-grants-1986_04 |