HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 3-(1-Piperazinyl)-1,2-benzisothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | 3-Chloro-1,2-benzisothiazole | HCID 598190 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 3-(1-Piperazinyl)-1,2-benzisothiazole | HCID 2772144 | 92.3% |
Reaction Steps
215.4 g (2.50 mol) of piperazine, 50.0 g of chlorobenzene, 100.0 g of ethylene glycol were placed in a four-neck 1000 ml flask equipped with a stirrer, a thermometer, a dropping funnel and a condenser, 169.5 g (1.00 mol) of 3-chloro-1,2-benzisothiazole was added dropwise in the melted state at about 120° C. over 1 hour while stirring, which was thereafter stirred for 2 hours to complete the reaction. After excess piperazine was removed with water, the reaction mixture was made acidic with hydrochloric acid, extracted into an aqueous layer, which was made alkaline with aqueous sodium hydroxide to obtain 202.4 g (m.p. 89°-90° C.) of 3-(1-piperazinyl)-1,2-benzisothiazole as crystals. Yield from 3-chloro-1,2-benzisothiazole was 92.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861511 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-ede2007e863e491c91da20a282468f06 |
| Source note | uspto-grants-1999_01 |