HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 13324092, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13324091 | HCID 13324091 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 13324092 | HCID 13324092 | 108.8% |
Reaction Steps
To a stirred mixture of CNBr (5.9 g, 0.056 mole), K2CO3 (8.6 g) and CHCl3 (80 ml) was added dropwise 3-(1-methyl-4-piperidinyl)-1,2-benzisothiazole (11.0 g, 0.051 mole) in CHCl3 (30 ml). The mixture was stirred and refluxed for 4 hours and thereafter cooled and filtered. The filtrate was concentrated in vacuo to a solid. The solid was triturated with hexane and collected to yield 13.5 g of the desired compound. Recrystallization from MeOH--H2O (twice) yielded 4.5 g (36%) of the benzisothiazole, m.p. 118°-120°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04528292 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-79db1c5b52ff4d72aec99cb44e7ee2a7 |
| Source note | uspto-grants-1985_07 |