HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 1-(4-Chlorophenyl)-1'-cyanospiro[indoline-3,4'-piperidine]
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4-Chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] | HCID 12801589 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Chlorophenyl)-1'-cyanospiro[indoline-3,4'-piperidine] | HCID 12801611 | — |
Reaction Steps
A mixture of 0.95 g of 1-(4-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] (Example 2), 0.42 g of cyanogen bromide and 1 g of potassium carbonate in 25 ml of dichloromethane is stirred at ambient temperature for two hours. The reaction mixture is filtered and the filtrate concentrated to dryness leaving an oily residue which is crystallized from an acetone-hexane mixture leaving colorless crystals, mp 178.5°-180° C. of 1-(4-chlorophenyl)-1'-cyanospiro[indoline-3,4'-piperidine].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04345081 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-5f456e272dc74fc3814653842416b157 |
| Source note | uspto-grants-1982_08 |