HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 21456041, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 12232368 | HCID 12232368 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 21456041 | HCID 21456041 | — |
Reaction Steps
10.1 g of 10-chloro- 10,11-dihydro-2-iodo-dibenzo[b,f]-thiepin and 23.3 g of piperazine are held at 120°-130° C for 1 hour. The mixture is cooled, diluted with 2-N sodium hydroxide and extracted with ether. The organic phase is washed with water until neutral and extracted with 500 ml of 2-N hydrochloric acid. The aqueous phase is made alkaline and extracted with chloroform. The organic phase is dried over magnesium sulphate and concentrated under reduced pressure. There is obtained 1-(10,11-dihydro-2-iodo-dibenzo[b,f]thiepin-10-yl)-piperazine as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006145 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-1b273d89c38440bfa1824fca95a1f7e3 |
| Source note | uspto-grants-1977_02 |