HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 15631610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 15631609 | HCID 15631609 | — |
| Product | HCID 15631610 | HCID 15631610 | — |
Reaction Steps
Dissolved in 20 ml of thionyl chloride was 1.76 g of 1-(2-furanylcarbonyl)-4-(2-hydroxyethyl)piperazine. The resulting mixture was stirred at room temperature for 7.5 hours. The thionyl chloride was distilled off under reduced pressure and the residue was poured into cold water. After alkalinization of the resulting aqueous solution with sodium carbonate, the solution was extracted with benzene and the benzene layer was washed with water. The benzene layer was dried over anhydrous magnesium sulfate and thereafter concentrated under reduced pressure to give 1.2 g of an oily substance. The reaction product was provided for the next step in its unpurified form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04876345 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-d511aea011ef45e290ab3558bab1095f |
| Source note | uspto-grants-1989_10 |